|Year : 2018 | Volume
| Issue : 1 | Page : 13-27
Current status of radiation countermeasures for acute radiation syndrome under advanced development
Vijay K Singh, Oluseyi O Fatanmi, Paola T Santiago, Madison Simas, Briana K Hanlon, Melissa Garcia, Stephen Y Wise
Division of Radioprotectants, Department of Pharmacology and Molecular Therapeutics, F. Edward Hébert School of Medicine, Uniformed Services University of the Health Sciences; Armed Forces Radiobiology Research Institute, Uniformed Services University of the Health Sciences, MD, USA
|Date of Web Publication||22-Jan-2018|
Prof. Vijay K Singh
Division of Radioprotectants, Department of Pharmacology and Molecular Therapeutics, F. Edward Hébert School of Medicine, Uniformed Services University of the Health Sciences; Armed Forces Radiobiology Research Institute, Uniformed Services University of the Health Sciences, MD
Source of Support: None, Conflict of Interest: None
The availability of safe and effective radiation countermeasures for the military and civilian population represents a significant unmet medical need. To expedite the development of countermeasures for life-threating situations, the United States Food and Drug Administration (US FDA) has implemented the “Animal Rule” which applies to the development and evaluation of drugs and biologics to reduce or prevent life-threatening conditions caused by exposure to lethal or permanently disabling agents where human efficacy trials are neither feasible nor ethical. In addition, the FDA has introduced several incentives (fast track, orphan drug status, and emergency use authorization [EUA]) to attract drug sponsors to develop such agents for human use. Repurposing is vital to make drugs available for life-threatening conditions. Drugs are commonly repurposed for new indications not originally envisioned. By repurposing a drug, it can be made available for human use much quicker, but this pathway also involves issues such as intellectual property rights as corporations are reluctant to expose their blockbuster pharmaceuticals to additional scientific scrutiny. Two radiomitigators for hematopoietic acute radiation syndrome (H-ARS) (Neupogen and Neulasta) have been approved by the FDA through repurposing. The EUA is a legal means for the FDA to approve new drugs or new indications for the previously approved drugs for use during a declared emergency and is a valid way to expedite drug development. Several promising agents with and without FDA investigational new drug (IND) status for ARS are under advanced development. In the next few years, we expect that the FDA will approve a few radioprotectors for H-ARS as well as gastrointestinal ARS via Animal Rule.
Keywords: Animal Rule, emergency use authorization, nonhuman primates, radiation, repurposing
|How to cite this article:|
Singh VK, Fatanmi OO, Santiago PT, Simas M, Hanlon BK, Garcia M, Wise SY. Current status of radiation countermeasures for acute radiation syndrome under advanced development. J Radiat Cancer Res 2018;9:13-27
|How to cite this URL:|
Singh VK, Fatanmi OO, Santiago PT, Simas M, Hanlon BK, Garcia M, Wise SY. Current status of radiation countermeasures for acute radiation syndrome under advanced development. J Radiat Cancer Res [serial online] 2018 [cited 2020 Dec 3];9:13-27. Available from: https://www.journalrcr.org/text.asp?2018/9/1/13/223744
| Introduction|| |
The threat of radiological and nuclear events is a critical concern for all government agencies involved in national security and public health preparedness. Radiation countermeasures that are safe, easily administered, and effective at reducing or eliminating adverse health consequences to individuals and the overall public health impact of radiation exposure are urgently needed. Though efforts have been ongoing for six decades to develop such agents, there has been limited success to have such agents approved by the United States Food and Drug Administration (US FDA) for human use. The development and availability of suitable radiation countermeasures for hematopoietic acute radiation syndrome (H-ARS) and gastrointestinal ARS (GI-ARS) remains a substantial unmet medical need and has been recognized as a high priority area by the government.
We have focused on medical countermeasures that are currently under advanced development and have been evaluated for efficacy in large animal models for a survival benefit. Such agents are expected to be assessed fully for their pharmacokinetics, toxicity, safety, and efficacy, with the expectation of being approved by the US FDA for use in humans. As discussed later, the nonhuman primate (NHP) is the most appropriate animal model for developing radiation countermeasures for ARS following the FDA Animal Rule. These agents will be approved by the FDA based on efficacy results from animal models. Their toxicity/safety will be studied in phase I studies once such agents obtain investigational new drug (IND) status.
Several drugs have received US FDA IND status, and an additional few agents are progressing well to soon receive IND status. IND filings are generally not indication-specific but product-specific. However, IND is filed to the relevant FDA division based on the first indication being studied by the sponsor. The same sponsor can study other indications under the same IND by cross-referencing the first IND (i.e. authorizing different divisions of the FDA to review the original IND). It is beyond the scope of this article to include all drugs that are presently being developed as potential radiation countermeasures, either against low doses of radiation or as anticancer drugs, agents which are used as dietary supplements, or other plant products which may not be regulated by the FDA for approval and marketing. We have focused on potential countermeasures that are being developed for either H-ARS or GI-ARS.
Here, we have discussed countermeasures that are being developed for H-ARS and GI-ARS. The majority of the agents discussed in this article have been investigated in the NHP model for efficacy against whole-body or partial-body irradiation. A few agents have shown promising efficacy in rodents and are ready to move forward to the NHP model for further investigation. One agent has been investigated using the canine model.
| Radiation Countermeasures under Advanced Development for Acute Radiation Syndrome|| |
Advanced development of radiation countermeasures implies the use of large animals for investigations for pharmacology, safety/toxicity, efficacy, and scaling to humans. There are currently nine radiation countermeasures with US FDA IND status. A few radiation countermeasures have demonstrated efficacy in large animal models in addition to small animals but have not yet achieved IND status. We have discussed agents that have US FDA IND as well as the agents that have been tested in NHPs and not yet received IND status. Emphasis has been given to survival benefits in NHP studies though other agents tested for improvement in cytopenia in NHPs receiving lethal doses of radiation are also included. Before discussing individual radiation countermeasures under the above categories, it is important to discuss some terminology used during the development of such agents following the US FDA Animal Rule. Though the discussed terminology is based on US agencies, other countries are coming up with similar pathways for the approval of medical countermeasures for chemical, biological, radiological, or nuclear (CBRN) threat agents.
| Animal Rule|| |
The US FDA Animal Rule applies to the development of drugs and biologics to reduce or prevent life-threatening conditions caused by exposure to lethal or permanently disabling CBRN agents where human efficacy studies are neither feasible nor ethical. The FDA may grant marketing approval to a drug under development if animal efficacy studies adequately establish that the drug will produce a clinical benefit in humans., The pharmaceutical agents being developed in this manner should follow the existing requirements for establishing the safety of new drugs. The FDA will rely on the animal efficacy studies if the following four criteria are met:
- The pathophysiological mechanism of injury/toxicity by the stimulus/agent and the role of the product in prevention or significant reduction of aforementioned injury/toxicity are well understood
- The efficacy of the product is demonstrated in more than one animal species with a response predictive of human response or a single animal species that has been satisfactorily characterized for predicting the human response
- The animal study endpoints clearly relate to the desired result in humans, normally reduced morbidity or mortality
- The effective dose can be calculated from kinetic and pharmacodynamics of the product (or relevant data) in both humans and animals.
It is reasonable to expect that a drug investigated in animals is to be indicative of human efficacy only when all above criteria are met. The Animal Rule is intended to be used in the development of drugs to counter debilitating or lethal conditions resulting from either accidental or deliberate exposure to CBRN agents.
Although no species are specified in the Animal Rule, only animals that can be scientifically justified in terms of key characteristics comparable to the human disease or condition should be used. Likewise, the mechanism by which the drug presents its effects should be understood to determine the appropriate dose and dose schedule for efficacy in humans.
There are additional requirements for drug approval through the Animal Rule:
- A plan outlining the approach to field studies that would evaluate the safety and clinical benefit of the drug, if such a study would be ethical or feasible (i.e. emergency event where the drug is administered)
- Restrictions regarding distribution, administration, and use, to ensure safety
- The package insert should include information that the drug was approved based solely on animal efficacy studies for ethical and feasibility reasons along with all other information the FDA requires at the time of approval. These details should be communicated before administering or dispensing the drug, if possible.
The drugs approved following the Animal Rule must follow postmarketing, record keeping, and safety reporting requirements. To date, only two radiomitigators for H-ARS have received FDA approval under the Animal Rule. No radioprotector has yet been approved by the FDA for H-ARS or GI-ARS.
| Orphan Drug Status|| |
The mission of the FDA's Office of Orphan Products Development is to advance the investigation and development of drugs or biologics that demonstrate potential for the treatment of rare diseases or conditions. The FDA provides incentives to sponsors to develop products for rare diseases. The orphan drug status benefit in the US is a 7-year period of market exclusivity for the indication if an agent gets approved by the FDA for human use. This program has successfully enabled the development and marketing of over 600 drugs and biologics for rare diseases since 1983 while fewer than 10 such agents came to market between 1973 and 1983. The Orphan Drug Designation program provides orphan status to drugs and biologics defined as those intended for the safe and effective treatment or prevention of rare diseases/disorders that affect fewer than 200,000 people in the US or that affect more than 200,000 persons but are not expected to recover the costs of developing the drug. The majority of radiation countermeasures under advanced development have received FDA orphan drug status.
| Fast Track|| |
Fast track is a process designed to facilitate the development and expedite the review process of drugs or biologics to treat a broad range of serious conditions and fill an unmet medical need. The purpose is to get promising new drugs to the patient as early as possible. Determining whether a condition is serious is a matter of judgment. It is generally based on the fact that the condition will have a negative impact on factors such as survival and day-to-day functioning if left untreated. Filling an unmet medical need is defined as providing a therapy where none exists or as providing a therapy which may be potentially better than available therapy. Any drug being developed to treat a condition with no current therapy is directed as an unmet need. If there are available therapeutics, a fast track drug must show advantage over available therapeutics. Fast track designation is requested by the drug sponsor and such request can be made at any time during drug development. The FDA reviews the request and decides within 60 days.
| Emergency Use Authorization|| |
The emergency use authorization (EUA) authority allows the FDA to strengthen the nation's public health protections against CBRN threats by expediting the availability and use of medical countermeasures required during public health emergencies. Under Section 564 of the Federal Food, Drug, and Cosmetic Act, the FDA may allow unapproved medical products or unapproved uses of approved countermeasures to be used in an emergency to treat or prevent life-threatening indications caused by CBRN threat agents when there are not enough alternatives approved and available.
Issuance of an EUA by the FDA requires several steps. First, one of the four following determinations must be in place: (a) the Department of Defense Secretary issues a determination of military emergency or significant potential for military emergency, (b) the Department of Homeland Security (DHS) Secretary issues a determination of domestic emergency or significant potential for domestic emergency, (c) the Department of Health and Human Services (HHS) Secretary issues a determination of public health emergency or significant potential for public health emergency, (d) the DHS Secretary issues a material threat determination.
Once one of the above four determinations is met, the HHS Secretary can issue a declaration that circumstances exist to justify issuing the EUA. This declaration is specific to EUAs and is not linked to other types of emergency declarations. The FDA Commissioner, in consultation with the HHS Assistant Secretary for Preparedness and Response, Control and Prevention, and the National Institutes of Health, can then issue the EUA if criteria for issuance under the statute are met. The FDA publishes a public notice of each EUA that is issued in the Federal Register.
| Repurposing|| |
Discoveries of the molecular basis of disease provide unique opportunities to translate research findings into therapeutics. However, new drugs approved by the FDA or other regulatory agencies take an enormous amount of time, money, and effort largely due to bottlenecks in the therapeutic development process. Such development involves a long and complicated path to approval that requires safety and toxicity evaluation as well as evidence of safe delivery and efficacy. It also requires convincing documentation to corroborate manufacturing and stability. It takes significant amounts of time and money to accomplish all requirements. Delays and regulatory barriers mean that the translation of a promising molecule into an approved drug often takes more than 14 years and up to a billion dollars in investment. It is crucial to advance strategies to reduce this time frame, decrease costs, and improve success rates. This is of paramount importance specifically regarding life-threatening situations, for which no appropriate countermeasures are available. Repurposing refers to studying drugs that are already approved to treat some indications and to explore if they are effective and safe to treat other indications. An already FDA-approved drug that is repurposed has a considerably truncated route to FDA approval, saving both time and money.
Agents approved for other indications have already been investigated in humans, so exhaustive information is available on their pharmacology, toxicity/safety, and mechanism of action. Further, approximately 80% of drugs that enter clinical trial are never approved by the regulatory bodies for human use. This suggests that for every five drugs that make it into the clinic, there are four that fail to demonstrate efficacy for the indication, for which the agent was designed to be approved. This high-failure rate leads to the availability of a large number of existing and partially developed candidate drugs with known pharmacology, toxicity/safety, formulation, and mechanism of action. Since repurposing builds upon earlier research and development efforts, candidate agents could be ready for other clinical indication studies sooner, accelerating their review and approval by the FDA, and ultimately their integration into health care. Both radiation countermeasures approved for H-ARS following the Animal Rule, Neupogen and Neulasta, are repurposed agents., Both agents were in the clinic for other indications. Currently, several agents such as Promacta, Pentoxifylline, Lova-, Sim-, Atorvastatin, Palifermin, Anakinra, Forteo, Cozaar, Increlex, Oprelvekin, Celecoxib, Mozobil, Neumega, Epogen, Surfaxin, Neurontin, and Metformin were previously approved for other indications and are being evaluated as radiation countermeasures for ARS and delayed effects of acute radiation exposure (DEARE). Some of these agents have demonstrated promising results as radiation countermeasures and are progressing well for the FDA approval.
| Investigational New Drug and New Drug Application/biologic License Application|| |
During the early preclinical development of a new drug, the primary goal of the sponsor is to determine if the agent is reasonably safe for initial use in humans during clinical studies and if the agent demonstrates pharmacological attributes that justify commercial development for a profit-making endeavor. When a drug candidate is recognized as a sustainable candidate for further development, the drug sponsor then concentrates on accumulating the data necessary to determine that the agent will not expose humans to excessive risks when used in limited and initial clinical studies.
An IND is a request for authorization from the FDA to administer an investigational drug or biologic to humans. Such authorization must be obtained before interstate shipment and administration of any new drug or biologic that is not the subject of an approved new drug application (NDA) or biologics license application (BLA) for biologics.
Once the IND is submitted to the FDA, the drug sponsor must wait 30 calendar days before initiating any clinical studies. During this period, the FDA has an opportunity to review the IND for safety to assure that research subjects will not be subjected to unreasonable risk resulting from drug administration.
There are three types of IND: (a) An investigator IND is submitted by a physician who both initiates and conducts an investigation and under whose immediate direction the investigational drug is administered or dispensed. A physician might submit a research IND to propose studying an unapproved drug or an approved product for a new indication or in a new patient population. (b) Emergency use IND allows the FDA to authorize use of an experimental drug in an emergency that does not allow time for the submission of an IND in accordance with 21 CFR, Sec. 312.23 or Sec. 312.20. It is also used for patients who do not meet the criteria of an existing study protocol or if an approved study protocol does not exist. (c) Treatment IND is submitted for experimental drugs demonstrating promise in clinical evaluation for serious or life-threatening conditions while the final clinical investigation is conducted, and the FDA review takes place.
The regulation of new pharmaceuticals has been based on the NDA in the US. Every new agent has been the subject of an approved NDA before the commercialization of the agent in the US. The NDA application is the vehicle through which the sponsor of any drug formally requests that the FDA approves a new agent for sale and marketing in the US. The data collected during the preclinical studies conducted in animal models and clinical trials in human of an IND become part of the NDA. For biologics, a BLA is equivalent to NDA.
The objectives of the NDA are to offer enough data and information to allow the FDA reviewer to reach the following: (a) whether the agent is safe and effective in its proposed use(s), whether the benefits of the agent outweigh the risks, (b) whether the proposed label of drug is appropriate and what such package insert should contain, (c) whether the methods used in manufacturing the drug and the controls used to maintain the drug's quality are sufficient to preserve the drug's identity, strength, quality, and purity.
| Nonhuman Primate Model of Acute Radiation Syndrome|| |
Various animal models are used in the development of radiation countermeasures to treat ARS. Of the various models, including rodents and swine, NHPs are essential for countermeasure development. NHPs and humans have a high degree of biological similarity, sharing around 95% DNA sequence homology. NHPs and humans also share similar physiological response pathways and targets relevant to human disease. Various NHP species are used in the biomedical research. The two most common species, Rhesus and Cynomolgus, are from the genus Macaca. Other species including the African green monkey (Chlorocebus aethiops), squirrel monkey (Saimiri spp.), and baboon (Papio spp.) are used as well.,, Recently, significant investigations have been conducted to study the effects of radiation exposure on various biomarkers using the baboon model.,,,,
There are numerous benefits associated with the NHP model: (1) NHPs share a similar organ structure with humans. (2) NHPs have a longer lifespan as compared to smaller animal models which enables long-term study. (3) NHPs are suitable for the assessment of GI symptoms such as vomiting while other models are not. (4) The NHP is a well-characterized animal model for the study of radiation injury and countermeasure efficacy. (5) NHPs share similar pathophysiology with humans. Despite all its advantages, this model also has some disadvantages: (1) Ethical considerations make the use of this animal model difficult. (2) Outbreeding of the NHP model results in more variations compared to other models such as the murine model. (3) There is inherently more risk of injury involved in the handling of NHPs. (4) The NHP model has a small litter size and takes a longer time to grow. (5) The hirsute nature of this model makes cutaneous studies difficult. (6) The NHP model involves a higher cost of procurement and care. Despite its disadvantages, the NHP is considered the gold standard as an animal model for FDA drug approval.
| Radiation Countermeasures With the United States Food and Drug Administration Investigational New Drug|| |
There are several radiation countermeasures with and without FDA IND, which are under investigation in the NHP model. The majority of recent studies evaluating new agents are not yet published, and data are unavailable. It is expected that such data will be available to the scientific community in due course of time. Some agents that have been investigated specifically as countermeasures for ARS are discussed below. We have also included the agents that are currently under evaluation or moving to the NHP model for investigation.
AEOL 10150 (a mesoporphyrin mimetic; C48H56C15 MnN12) is a novel agent currently being developed as a countermeasure against the pulmonary effects of ARS and DEARE. This agent is a well-tolerated, broad-spectrum catalytic antioxidant capable of extending survival benefit and minimizing acute pathology as demonstrated by the studies administering subcutaneous (sc) daily treatments for 28 days to both mice and NHPs. Effective dosing for this drug has been recently explored using radiation-induced lung injury in the murine model (whole-thorax lung exposure with 14.6 Gy) of CBA/J mice. Beyond using this drug to counter high radiation dose pulmonary injury, this agent is also being investigated as a potential countermeasure for GI-ARS.
Investigation in NHPs demonstrated that AEOL 10150 administration reduced lung injury and increased survival after 11.5 Gy whole-thorax lung lethal dose (LD100/180) radiation exposure. Daily administrations of AEOL 10150 (5 mg/kg, sc) initiated 24 h postirradiation spared 26% of the treated animals from lung injury that would have been otherwise fatal (100% death in control group). Furthermore, CT scans revealed less pulmonary injury (pneumonitis, fibrosis, and effusions) in the AEOL 10150-treated animals at 60 days postirradiation. In a recent study, NHPs received 10.74 Gy whole-thorax lung irradiation (WTLI) using 6 MV linear accelerator-derived photons. The study comprised four cohorts: one control and three AEOL 10150-treated groups (n = 20/cohort). AEOL 10150 was administered daily sc at 5 mg/kg in each of three schedules, beginning 24 ± 2 h postirradiation: from day 1 to 28, from day 1 to 60, or a divided regimen from day 1 to 28 plus day 60 to 88. Control animals received 0.9% saline injections from day 1 to 28. All animals received full supportive care and were followed for 180 days. A survival relationship was observed with the AEOL 10150 treatment and time after lethal WTLI. Analysis of survival curves suggested that treatment efficacy could be increased by extending the treatment schedule to 90 days or longer after WTLI. No survival improvement was noted in the AEOL 10150 cohorts treated from day 1 to 28 or using the divided schedule of day 1–28 plus day 60–88. These results suggest that AEOL 10150 may be an effective countermeasure against lung injury.
Genistein (4', 5, 7-trihydroxyisoflavone) is a soy-derived isoflavone with selective estrogen receptor activation, protein tyrosine kinase inhibition, antioxidant, and free radical scavenging activities., Genistein can act as both a radioprotector and a radiomitigator. BIO 300 is an aqueous nanosuspension consisting of synthetic genistein that is manufactured using a proprietary nanomilling process that significantly reduces the genistein particle size. This formulation has several key advantages including improved bioavailability and ease of administration. Initial preclinical study carried out at the Armed Forces Radiobiology Research Institute using murine models established genistein's radioprotective efficacy. A single dose of BIO 300 significantly improved 30-day survival in mice exposed to 9.25 Gy 60Co γ-radiation. BIO 300 underwent further development as a radiomitigator for ARS and DEARE at Humanetics Pharmaceuticals. Genistein, used as a mitigator, was reported in clinical trials to reduce adverse effects of chemotherapy and radiotherapy., In a murine model of ARS, genistein protected bone marrow progenitor cells from radiation-induced injury, leading to prevention of hematopoietic stem cell pool exhaustion, and thereby augmenting subsequent recovery of blood neutrophil and platelet levels.,, Genistein also increased murine survival after thoracic irradiation. Several mechanisms have been proposed for the radioprotective efficacy of genistein, including activation of the DNA repair enzyme, quiescence of the cell cycle of Lin - cells in the G0/G1 phase in vivo, and the suppression of inflammation. Currently, BIO 300 is being investigated for pharmacokinetics and efficacy in NHPs as a radioprotector against total-body 60Co γ-irradiation when administered sc or per os (po).
A truncated version of flagellin, Entolimod, retains its radioprotective efficacy and stability without its immunogenic properties. Entolimod acts as an agonist of toll-like receptor 5 and triggers nuclear factor-kB signaling that drives expression of numerous genes, including inhibitors of apoptosis, scavengers of reactive oxygen species, and a cascade of protective or regenerative cytokines. Granulocyte colony-stimulating factor (G-CSF) and interleukin-6 (IL-6) have been identified as biomarkers to assess Entolimod efficacy. Both cytokines were found to play significant roles in its mechanisms pertinent to enhanced survival in irradiated mice. The administration of antibody to either G-CSF or IL-6 effectively abrogates the radioprotective efficacy of Entolimod in irradiated mice.
Entolimod has been shown to be effective against both H-ARS and GI-ARS in mice as well as NHPs, acting as both radioprotector and radiomitigator., Entolimod treatment reduces apoptosis and accelerates crypt regeneration in the GI tract. These attributes make Entolimod a potentially useful countermeasure for both civilian and military personnel alike. The FDA has granted IND, fast track, and orphan drug status to Entolimod as a radiation countermeasure. Clinical studies with healthy human volunteers demonstrated that Entolimod is systemically well tolerated and had biomarker results corresponding to the previous biomarker data from animal models of ARS.,, A pre-EUA dossier for Entolimod has been submitted to the FDA for review. Its sponsor, Cleveland BioLab, Inc., continues to discuss requirements for submission of a BLA.
Ex-RAD (a chlorobenzylsulfone derivative) is a small-molecule kinase inhibitor, and it provided significant protection against 60Co γ-irradiation when administered sc (500 mg/kg) to C3H/HeN mice 24 h and 15 min before irradiation, with a dose reduction factor of 1.16. Ex-RAD also demonstrated a significant survival benefit after prophylactic po administration. This drug accelerated the recovery of peripheral blood elements in irradiated mice when administered either sc or po., Ex-RAD manifests its protective effects through the upregulation of phosphatidylinositol 3-kinase/Akt (serine/threonine kinase, protein kinase B) pathways in cells exposed to radiation. Effective po administration makes Ex-RAD a potentially interesting and useful countermeasure that might be used to treat first responders as well as at-risk civilian populations in the event of a nuclear accident. NHP studies have been initiated in our laboratory to investigate its radioprotective and radiomitigative potential when administered either sc or po.
| Granulocyte-Macrophage Colony-Stimulating Factor/ Leukine/sargramostim|| |
Leukine has the FDA approval for five indications, three of which relate to the acceleration of neutrophil recovery in myelosuppressed patients. Leukine has been used to treat 14 radiation-exposed victims in three different accidents (dose range of 2.4–8.1 Gy), of whom nine survived., Although Leukine would certainly be utilized in cases of major radiological exposure contingencies and is well recognized to be effective in treating ARS, it has not been fully approved by the FDA for the specific treatment of ARS. The radioprotective efficacy of Leukine has been evaluated in mice, canines, and NHPs.,,, Unlike G-CSF, GM-CSF is species-specific. Recombinant human and canine GM-CSF have been used in NHP and canine studies, respectively.
GM-CSF enhances the recovery of white blood cells in different strains of mice, canines, and NHPs when administered either alone or in combination with other cytokines., Results consistently support recovery from severe neutropenia as an advantage of using GM-CSF in H-ARS. In murine and canine studies where the effectiveness of G-CSF and GM-CSF has been compared, G-CSF was found to be more effective in protecting irradiated animals., Recently, GM-CSF has been evaluated as a radiomitigator in NHPs and found to significantly improve survival when administered 48 h postirradiation (7 μg/kg/day, sc, number of doses depended on neutrophil counts) with minimal supportive care (i.e. Baytril antibiotic and no blood products) against two different doses of radiation (6.55 Gy and 7.18 Gy). It is important to note that G-CSF was not effective when evaluated in the absence of full supportive care (blood products). Sanofi is preparing a supplemental BLA submission to the FDA.
HemaMax has been shown to enhance mouse survival when administered as a single dose, either 24 h before or 1 h or 24 h after total-body irradiation (TBI). Neumedicines is developing HemaMax as a radiomitigator for the treatment of H-ARS and is planning a BLA submission to the FDA in the near future. Allometrically equivalent doses of mouse and human IL-12 have comparable pharmacokinetics. IL-12 administration significantly increased NHP survival in the study without supportive care when administered through parenteral route 24 h postirradiation.
A clinical phase-Ib safety study evaluating the predicted effective human dose has indicated that HemaMax is safe and well tolerated. Phase II equivalent data demonstrated that single administration of HemaMax significantly enhanced survival and reduced neutropenia/thrombocytopenia in NHPs when injected 24 h post-TBI, promoted immune functions, and possibly GI functions within acutely irradiated animals.,,
Myeloid progenitor cells
Myeloid progenitor cell (MPC) has been investigated for its use as a bridging therapy for radiation injuries and to mitigate the effects of lethal doses of 60Co γ-radiation and X-rays in different strains of mice. Pooled allogeneic MPC from AKR, C57Bl/6, and FVB mice was administered intravenously into haplotype-mismatched recipient BALB/c or CD2F1 mice at different time points after irradiation to evaluate the effect of MPC administration on survival in mice. The cryopreserved allogeneic MPC significantly protected both strains of mice irradiated with lethal doses of 60Co γ-radiation. The survival benefit in mice was MPC-dose-dependent and significant even when administered 7 days postirradiation. In addition, MPC administration decreased deaths from ARS at radiation doses as high as 15 Gy in CD2F1 mice. The histopathology of GI tissue from irradiated and MPC-injected mice demonstrated improved gut architecture compared to untreated controls. The effect of MPC administration on bacterial translocation from the GI to the heart, spleen, and liver in irradiated mice was also investigated by bacterial colony cultures and measuring endotoxin levels in serum samples. MPC decreased bacterial infection and inhibited endotoxin levels in serum. The results of these studies support administration of MPC as a bridging therapy, not only for the hematopoietic system but also for GI-ARS. Cellerant Therapeutics, Inc. (San Carlos, CA, USA) is developing a cell-based therapy containing human myeloid progenitors, CLT-008. This agent has received US FDA IND status (Cellerant Therapeutics – personal communication). Derived from adult hematopoietic stem cells, CTL-008 can produce functional granulocytes, red blood cells, and platelets in vivo. It is currently under clinical studies.
Neumune (androst-5-ene-3β,17β-diol) was the first radiation countermeasure for ARS to receive the FDA IND status. It was evaluated as both a radioprotector and a radiomitigator in murine and NHP models.,, Single administration of Neumune, either before or after a lethal dose of whole-body 60Co γ-radiation exposure, significantly enhanced mice survival, though postirradiation drug administration was less effective than preirradiation administration.,, The radiomitigator efficacy of Neumune was confirmed with both mouse and NHP models., Neumune significantly increased G-CSF and IL-6 in mice. Neutralization studies demonstrated that G-CSF was partially responsible for its radioprotective efficacy in mice., Clinical trials suggest that administration of Neumune may be a safe and effective method to stimulate innate immunity and alleviate ARS-associated neutropenia and thrombocytopenia. The development of this countermeasure remains uncertain. The Department of HHS decided not to purchase Neumune from Hollis-Eden citing that it was “technically unacceptable” and not in competitive range. As a result, Hollis-Eden (now Harbor Biosciences) decided to discontinue the development of Neumune.,
OrbeShield is a potent, topically active corticosteroid under development as an orally administered radiation countermeasure for GI-ARS. Beclomethasone 17,21-dipropionate demonstrated significant survival benefit in a canine model of GI-ARS. Canines received TBI, followed by autologous bone marrow administration and supportive care. There were three groups in this study: one control group and two OrbeShield-treated groups; both groups underwent different treatment schedules. Both OrbeShield-treated groups had higher survivors compared to the control group, indicating that OrbeShield can rescue inflamed tissues of the GI mucosa after irradiation, leading to improve survival benefits when drug treatment is initiated as late as 24 h postirradiation. OrbeShield has received IND, orphan drug, and fast track statuses from US FDA. No reports exist regarding its toxicity and pharmacokinetics in humans. OrbeShield is available in the US as the active pharmaceutical ingredient in a nasal spray and inhaler used for the treatment of asthma and allergic rhinitis. This property may be helpful for the development of this agent as a countermeasure. Although we have not come across any published result in NHPs, such studies may be being conducted currently.
| Radiation Countermeasures Without the United States Food and Drug Administration Investigational New Drug|| |
There are several promising radiation countermeasures that do not have FDA IND status yet but are moving forward with NHP studies. Some of these agents are discussed below.
| Gamma-Tocotrienol|| |
Gamma-tocotrienol (GT3) has comparable radioprotective efficacy and appears to be better than other tocols as a radioprotectant based on its evaluation in the murine model of ARS., GT3 is an inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme A reductase  and is being developed as a radioprotector for military and civilian use. Its radioprotective studies in murine model have been reviewed recently.
We have conducted a proteomics study of serum and jejuna samples from irradiated mice-administered GT3. These samples were analyzed by high-performance two-dimensional difference in gel electrophoresis, matrix-assisted laser desorption/ionization time of flight tandem mass spectrometry, and database for annotation, visualization, and integrated discovery (DAVID). Lysates were labeled with two different Cy dyes (Cy3 or Cy5); as an internal control, lysates from vehicle- and GT3-treated groups were pooled and labeled with Cy2 [Figure 1].
|Figure 1: 2D-DIGE analysis of GT3-treated and 11 Gy irradiated murine jejuna sample vs healthy murine jejuna sample. Overlay of two representative images from Healthy (Cy3, green) and irradiated GT3- treated (Cy5, red) mice. Spots are circled and numbered to correspond with proteins showing changes between treatments|
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When jejuna lysate from healthy mice were compared to irradiated mice exposed to 11 Gy and treated with either vehicle or GT3, 142 and 21 proteins, respectively, were differentially expressed (including isomers of the same proteins). In brief, GT3 treatment reduced the number of proteins altered by irradiation, making them more closely resemble the response of healthy animals. Similar observations have been made in ongoing transcriptomic study of NHP brain tissue (unpublished observation) and recently published microRNA (miRNA) results with NHP serum samples. The jejunal lysate from irradiated and vehicle-treated mice compared to that of irradiated and GT3-treated mice demonstrated 65 differentially expressed proteins. When serum proteins were compared between healthy mice and mice irradiated with 11 Gy and treated with either vehicle or GT3, 54 proteins were differentially expressed in vehicle-treated animals compared with 129 proteins differentially expressed in GT3-treated animals. The serum proteins from irradiated, vehicle-treated mice compared to that of irradiated GT3-treated mice demonstrated 91 proteins differentially expressed.
The proteins identified as being differentially expressed were uploaded to the DAVID software. Ingenuity pathway analysis (IPA, Ingenuity Systems, Redwood City, CA, USA) was then used to integrate the proteins into pathways and networks based on biological and/or functional relevance to the other proteins as well as the significance value of uploaded proteins. The IPA of the jejuna proteins yielded five top canonical pathways: calcium signaling, actin cytoskeleton signaling, epithelial adherens junction signaling, RhoGDI signaling, and a granulocyte adhesion and diapedesis. The top network-associated functions are cell signaling, posttranslational modification, and protein synthesis [Figure 2]. The IPA of the serum proteins yielded 5five top canonical pathways: acute phase response signaling, liver X receptor/retinoid X receptor (RXR) activation, farnesoid X receptor/RXR activation, complement system, and coagulation system. The top network-associated functions are free radical scavenging, metabolic disease, and humoral immune response [Figure 3]. In addition, we also performed similar proteomic analysis on another tocol radiation countermeasure that is under evaluation, tocopherol succinate. The results with jejunum of mice exposed to 9.2 Gy of this analysis are presented in [Figure 4], [Figure 5], [Figure 6]. We have conducted similar study in mice exposed to 11 Gy (data not presented) and these results support data with 9.2 Gy.
|Figure 2: Top network of murine jejuna proteins differentially expressed in response to GT3 treatment (200 mg/kg, sc) after exposure to 11 Gy 60Co γ-radiation yielded by IPA with Hub and Spoke analysis. From the top differentially expressed proteins that are protected by GT3, proteins were up-regulated (red color) and down-regulated (green color) by GT3. These are found in the set of proteins significantly (p<0.05) affected by GT3|
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|Figure 3: Top network of murine serum proteins differentially expressed in response to GT3 treatment (200 mg/kg, sc) after exposure to 11 Gy 60Co γ-radiation yielded by IPA with Hub and Spoke analysis. From the top differentially expressed proteins that are protected by GT3, proteins were up-regulated (red color) and down-regulated (green color) by GT3. These are found in the set of proteins significantly (P < 0.05) affected by GT3|
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|Figure 4: 2D-DIGE analysis of TS-treated and 9.2 Gy irradiated murine jejuna samples vs healthy murine jejuna samples. Overlay of two representative images from Healthy (Cy3, green) and irradiated TS- treated (Cy5, red) mice. Spots are circled and numbered to correspond with proteins showing changes between treatments|
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|Figure 5: Top network of murine jejuna proteins differentially expressed in response to TS treatment (400 mg/kg, sc) after exposure to 9.2 Gy 60Co γ-radiation yielded by IPA with Hub and Spoke analysis. From the top differentially expressed proteins that are protected by TS, proteins were up-regulated (red color) and down-regulated (green color) by TS. These are found in the set of proteins significantly (p<0.05) affected by TS|
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|Figure 6: Top network of murine jejuna proteins differentially expressed in response to TS treatment (400 mg/kg, sc) after exposure to 11 Gy 60Co γ-radiation yielded by IPA with Hub and Spoke analysis. From the top differentially expressed proteins that are protected by TS, proteins were up-regulated (red color) and down-regulated (green color) by TS. These are found in the set of proteins significantly (p<0.05) affected by TS|
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GT3 has been investigated for its radioprotective efficacy against 60Co γ-irradiation using an NHP model with encouraging results. GT3 helped in the recovery of radiation-induced thrombocytopenia and neutropenia in irradiated NHPs compared to the vehicle controls; these results were especially significant after lethal exposures to 5.8 or 6.5 Gy 60Co γ-TBI. The stimulatory effect of GT3 on platelets and neutrophils was positively and directly correlated with radiation dose; the 75 mg/kg dose was more effective compared to a dose of 37.5 mg/kg. GT3 was also effective against 6.5 Gy whole-body γ-irradiation in improving platelet and neutrophil counts. Furthermore, a single dose of GT3, without any supportive care, was comparable to multiple doses of Neupogen and two doses of Neulasta with full supportive care (including blood products) in terms of improving hematopoietic recovery in the NHP. Using the NHP model, it was demonstrated that three miRNAs correlated with the radioprotective efficacy of GT3. These miRNAs in GT3-treated and irradiated NHPs resembled the unirradiated animals: miR-30a, miR-126, and miR-375.
Global metabolomic and lipidomic changes have been analyzed in serum samples of unirradiated NHP-administered GT3. Our study demonstrates that alterations in metabolites manifest only 24 h after GT3 administration. Furthermore, metabolic changes are associated with a transient increase in the bioavailability of antioxidants, including lactic acid, cholic acid, and anti-inflammatory metabolites, 3 deoxyvitamin D3 and docosahexaenoic acid. In addition, our pilot study using irradiated NHPs demonstrated several metabolites that are altered after radiation exposure, including compounds involved in fatty acid-β oxidation, purine catabolism, and amino acid metabolism. Primary metabolites validated included amino acids, carnitine/acylcarnitines, creatine, and xanthine. GT3 administration reduced high fluctuations in serum metabolite levels, demonstrating a beneficial effect on animals exposed to radiation. This initial assessment also highlights the utility of metabolomics and lipidomics to determine the underlying physiological mechanisms involved in the radioprotective efficacy of GT3.
As a adrenoreceptor agonist, indralin exerts its radioprotective efficacy through activation of α1(B)-adrenoreceptors, members of G-protein-coupled receptors. Its radioprotective efficacy has been evaluated in seven animal models (mice, rats, hamsters, guinea pigs, rabbits, canines, and NHPs), and it demonstrated consistent efficacy., Its efficacy was investigated in NHPs using whole-body 60Co γ-radiation. Animals received a dose of 6.8 Gy radiation with 100% lethality in control over 30 days. Indralin (40–120 mg/kg) was administered intramuscularly 5 min before irradiation. At a dose of 120 mg/kg, it protected five out of six NHPs compared with the control group in which all 10 animals died. Indralin decreased radiation-induced injuries in NHPs, mitigating the effects of ARS. The therapeutic index for indralin, the ratio of the maximum tolerated dose to the average effective dose, was 10. These results demonstrate that indralin has promising radioprotective efficacy and has a high therapeutic index.
| Placental-Derived Cellular Therapy (Plxr18)|| |
PLX-R18 cells are three-dimensional-expanded placenta-derived cells with the ability to protect and regenerate bone marrow. These cells secrete several cytokines including G-CSF, IL-6, monocyte chemoattractant protein-1, and growth-regulated oncogene (also known as keratinocyte chemoattractant), which participate in reconstitution of hematopoietic system  and provided survival benefit in irradiated C3H/HeN mice. PLX-R18 helps in recovery of white blood cells, red blood cells, and platelets in irradiated animals. Recently, PLX-R18 was investigated in irradiated NHPs as an intramuscular injection. Although the sample size in the NHP study was small (six or seven NHPs/group), all PLX-R18-treated NHP groups (4, 10, and 20 million cells/kg) demonstrated improved survival as compared to untreated group where mortality was 50%. This agent has been granted orphan drug status by the US FDA. In unirradiated animals, these cells do not increase CBC in recipient animals, suggesting that this agent can be given to probable radiation exposed victims without assessing the radiation dose.
| Alpha-Methyl Hydrocinnamate (St7 and Its Isomer St7-S)|| |
Alpha-methyl Hydrocinnamate (ST7) extends signal transducer and activator of transcription 5 phosphorylation, reduces growth-factor dependence of multi-lineage cells, and accelerates erythropoiesis. ST7 and its isomer (ST7-S) were studied for their effects on myeloid progenitors and hematopoietic stem cells following irradiation in NHP and mice models. Addition of ST7 or ST7-S increased granulocyte macrophage colony-forming unit production, reduced neutrophil apoptosis, and enhanced hematopoietic stem cell survival postradiation. ST7 and ST7-S administered in normal baboons increased neutrophil and platelet counts by 50%–400%. Collectively, the studies indicate that ST7 and ST7-S enhance myeloid recovery postradiation and merit further evaluation to accelerate hematologic recovery and survival benefit after irradiation.
Irradiation causes the release of acid sphingomyelinase within minutes to the outer endothelial plasma membrane where it finds its substrate, sphingomyelin, and generates the pro-apoptotic second messenger, ceramide. Ceramide assembles a signaling platform on the endothelial surface that mediates apoptosis, and coupling of microvessel injury to direct intestinal stem cell (ISC) damage coordinately determines ISC survival from irradiation. The antagonism of ceramide on the irradiated endothelial surface prevents the formation of ceramide-rich platforms required for endothelial death, thereby protecting mice against GI-ARS lethality. Anticeramide monoclonal antibody binds to ceramide, preventing the formation of signaling platforms, protecting the cell and tissue from radiation-induced apoptosis. This protective process appears to facilitate the recovery of crypt stem cell clonogens in GI tissue of radiation-induced GI-ARS. Anticeramide antibody has been reported to protect C57BL/6 mice when administered prophylactically via intravenous infusion 15 min before radiation exposure (15 Gy, 2.12 Gy/min) with a 137Cs source. This agent has been extensively studied in our laboratory over several years and demonstrated remarkable efficacy against GI-ARS (unpublished observation). Anticeramide antibody represents a new class of radiation countermeasures that may be effective against radiation-induced GI-ARS. This agent is expected to be evaluated for its pharmacokinetics and efficacy NHPs soon.
In addition to the above countermeasures, several other agents have been tested in NHPs in the past. Neupogen and Neulasta's approval as countermeasures for H-ARS is based on efficacy testing in NHPs., Several cytokines such as IL-3, IL-6, leukemia inhibitory factor, stem cell factor, Fms-related tyrosine kinase 3 ligand, and megakaryocyte growth and development factor have been tested for survival benefit or hematopoietic recovery in irradiated NHPs.,,,,,,,,,,,
| Conclusion and Future Direction|| |
From the US and global perspectives, biomedical research concerning medical countermeasure development for life-threatening conditions is quite robust in the US as well as in some other countries, mainly due to greater government funding following the 9/11 incidence and subsequently significant rise in terrorist-associated threats. Unfortunately, only a limited number of radiation countermeasures have been fully approved by the US FDA. Nine radiation countermeasures have received FDA IND status, and three agents mitigating radiation injury, Neupogen, Neulasta, and Leukine, have already been procured by the US government for the vendor-managed inventory.
Although significant progress has been made in radiation countermeasure development over the last several years, additional effort is required to push new promising agents through the regulatory pipeline for early approval. This approval pipeline for new promising agents appears to be unreasonably slow and cumbersome.
The dearth of FDA-approved radiation countermeasures has prompted intensified search for a new generation of radiation countermeasures. Several promising radiation countermeasures, particularly for ARS, are currently moving forward with continued support and effort by both governmental agencies and publicly and privately owned pharmaceutical companies. There are a limited number of countermeasures that are moving well following the FDA Animal Rule and may be approved soon. Such effort will close the gap of this critically important, unmet need of radiation countermeasures.
We completely recognize that our listing of drugs being investigated in NHP model may not be exhaustive and up to date due to the lack of accessibility to recently generated data with potential radiation countermeasures. Such inaccessibility is due to the vested financial interests of the pharmaceutical companies in protecting potentially marketable agents. Issues of confidentiality and the “intellectual property rights” of pharmaceutical companies and government agencies, particularly the US FDA, also limit accessibility. We have mentioned few agents for which NHP data is not available, but we expect that such agents are under investigation in NHPs. Although significant progress has been made, additional effort is still needed.
The FDA has not yet approved any agent for use as a radioprotector for H-ARS following the Animal Rule. Both FDA-approved agents for H-ARS are radiomitigators. Further, no drug has been approved for GI-ARS, either as a radioprotector or as a radiomitigator. There are several reasons for such failure. Some important issues are the shortage of multiple large animal models that represent the pathophysiology of humans for studying radiation injury and the lack of corporate interest for the development of such agents. The development of such agents will have a small market, limiting the revenue generation to offset the investment on such agent's FDA approval. The FDA Animal Rule emphasizes a good understanding of the pathophysiology of radiation injury, a well-understood mechanism of action of agents under development, and the identification of biomarkers for drug dose conversion (animal to human) and to also serve as a predictive marker for the efficacy in humans. Accomplishing these tasks for FDA approval is not easy, and as a result, several radiation countermeasures at advanced stages of development remain stagnant for significant periods of time. Due to such hurdles, the corporate entity loses interest for the development of such agents. These issues emphasize the need for a combined effort between academia, corporate partners, and government agencies. The FDA has come out with various options to attract corporate partners, but these incentives may not be enough to keep corporate partners interested.
Repurposing the FDA-approved drugs for another indication is reasonable approach to save money and time and to avoid excessive risks associated with new drug development and approval. Such an approach requires attention from scientists as well as funding agencies. The Radiation Countermeasure Program of National Institute of Allergy and Infectious Diseases as well as Biomedical Advanced Research and Development Authority has supported repurposing efforts with several agents expected to be approved as radiation countermeasures. Although the traditional pathway of radiation countermeasure development must be supported, repurposing should also be explored. There are many agents that have dual use and are being investigated as radiation countermeasures for GI-ARS as well as for H-ARS. Further, combinations of different agents are being tested where one agent is already approved by FDA for another indication. There are studies in recent past using combinations of two drugs for additive efficacy.
The opinions or assertions contained herein are the private views of the authors and are not necessarily those of the Armed Forces Radiobiology Research Institute, the Uniformed Services University of the Health Sciences, or the Department of Defense. Mention of specific therapeutic agents does not constitute endorsement by the US Department of Defense, and trade names are used only for clarification. We gratefully acknowledge the research support from the National Institute of Allergy and Infectious Diseases (AAI-12044-0000-05000, Work Plan G) and Congressionally Directed Medical Research Programs (W81XWH-15-C-0117, JW140032) of the US Department of Defense to VKS. We also appreciate the help of Mr. Joshua Starr for IPA. We apologize to those having contributed substantially to the topics discussed herein that we were unable to cite because of space constraints.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
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[Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5], [Figure 6]
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