News

Kaléo Announces First U.S. Department of Defense Supply Contract for the Rapid Opioid Countermeasure System (ROCS) Antidote for Ultra-Potent Weaponized Opioids

Kaléo, a privately held commercial-stage U.S. pharmaceutical company, announced the execution of the first contract with the U.S. Department of Defense (DoD) for the procurement of the Rapid Opioid Countermeasure System (ROCS), a 10 mg Naloxone Auto-injector (naloxone hydrochloride injection) antidote for ultra-potent weaponized opioids. The contract includes an award for the manufacture and delivery of up to 788,000 units.

“ROCS was developed to protect and maintain the readiness of the Joint Force and our NATO allies,” said Colonel Matthew Clark, PhD, PMP, the Joint Project Manager for CBRN Medical. “Weaponized synthetic opioids, such as fentanyl and carfentanyl, have been used operationally in the past and continue to pose a unique threat to our service members. This first delivery of ROCS auto-injectors is a great achievement.”

Kaléo was awarded the prototype development contract for the ROCS program in 2018 by the Joint Project Manager for Chemical, Biological, Radiological, and Nuclear Medical (JPM CBRN Medical), a component of the U.S. Department of Defense’s Joint Program Executive Office for Chemical, Biological, Radiological, and Nuclear Defense (JPEO-CBRND) in collaboration with the Chemical and Biological Defense Program (CBDP). The JPM CBRN Medical facilitates the advanced development and acquisition of medical countermeasures (MCM) and systems to enhance the nation’s CBRN response capability.

“This first DoD procurement contract is a major milestone for Kaléo,” said Mark A. Herzog, the company’s vice president, global corporate affairs, defense and homeland security. “We are pleased to have delivered ROCS under budget, and five months ahead of schedule, despite challenges presented by the pandemic and disruptions to the global supply chain.”

Approved by the U.S. Food and Drug Administration (FDA) on February 28, 2022, ROCS is a 10 mg Naloxone Auto-injector (naloxone hydrochloride injection) indicated for the emergency treatment of people 12 years of age and older where use of high-potency opioids such as fentanyl analogues as a chemical weapon, is suspected. See full indication below.

Additionally, the Naloxone Auto-injector 10 mg is indicated for the temporary prevention (prophylaxis) of either breathing problems (respiratory depression), decreased brain and nerve function (central nervous system depression), or both, in military personnel and chemical incident responders entering an area contaminated with high-potency opioids such as fentanyl analogues.

The New Drug Application for the Naloxone Auto-injector 10 mg was submitted on August 31, 2021 and was granted Fast Track Designation by the FDA. In addition to more than 150 performance verification tests, the ROCS Naloxone Auto-injector 10 mg underwent military standard testing and evaluation for suitability on behalf of the JPM CBRN Medical which included three cumulative shock tests and seven cumulative environmental tests. The ROCS Naloxone Auto-injector 10 mg also meets the U.S. Food and Drug Administration (FDA) draft guidance standard for 99.999% device reliability.

 

Click here to learn more.

Recent News

04/19/2024

ivWatch prevents IV leakage events at Frimley Health

Frimley Health NHS Foundation Trust has found that 100% of IV leakage incidents were prevented by a proprietary patient monitoring system from ivWatch, which could potentially save patients the pain or discomfort of adverse IV events. The initial two-week phase of the study, which was published in the British Journal of Nursing, found that continuous

04/17/2024

U.S. Department of Health and Human Services Awards Kaléo with Contract to Develop Next Generation Organophosphate Nerve Agent Poisoning Countermeasure

Kaléo, a privately-held U.S. pharmaceutical company today announced their selection by the Biomedical Advanced Research and Development Authority (BARDA), part of Administration for Strategic Preparedness and Response (ASPR) within the U.S. Department of Health and Human Services (HHS), to develop the latest generation pralidoxime chloride auto-injector as a countermeasure against organophosphate or nerve agent poisoning.

04/15/2024

Activation Capital Welcomes Dr. Jim Pannucci as its Vice President of Entrepreneurship

Activation Capital, an innovation ecosystem development organization, announced today that it has appointed Jim Pannucci, Ph.D., PMP as its Vice President of Entrepreneurship. As the new Vice President of Entrepreneurship, Dr. Pannucci will help Activation Capital continue to grow a deep talent base of life sciences entrepreneurs operating in the region and help empower them