SOUTH SAN FRANCISCO, Calif., July 5, 2022 /PRNewswire/ — Titan Prescription drugs, Inc. (NASDAQ: TTNP) (“Titan” or the “Corporate”) lately introduced that the U.S. Meals and Drug Management (“FDA”) has cleared its Investigational New Drug (“IND”) software for a Section 1 learn about of its six-month or longer subdermal components of nalmefene, an opioid antagonist, supposed for the prevention of relapse following opioid cleansing in adults with Opioid Use Dysfunction (“OUD”).
Kate Beebe DeVarney, Ph.D., President and Leader Running Officer of Titan, commented, “FDA clearance of the IND for our ProNeura®-based nalmefene implant marks the most important milestone in growing a unique product that can lend a hand solution the decision for long-term remedy choices in habit drugs. We’re very thankful for the enhance we gained from the Nationwide Institute for Drug Dependancy, or NIDA, that enabled us to satisfy this function.”
About Titan Prescription drugs
Titan Prescription drugs, Inc. (NASDAQ:TTNP), founded in South San Francisco, CA, is a construction degree corporate growing proprietary therapeutics with its ProNeura® long-term, steady drug supply generation. The ProNeura generation has the prospective for use in growing merchandise for treating various continual stipulations, the place keeping up constant, around-the-clock blood ranges of medicine might benefit the affected person and toughen clinical results. In December 2021, Titan commenced a procedure to discover and overview strategic choices to improve shareholder price.
For more info about Titan, please talk over with www.titanpharm.com.
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