News

Serpin Pharma Secures $2 Million NCI Grant for Innovative Neuropathy Treatment

Serpin Pharma, a Virginia-based biopharmaceutical company, is proud to announce that it has been awarded a $2 million Phase II Small Business Innovation Research (SBIR) grant from the National Cancer Institute (NCI).

This grant will support the clinical development of SP16-3M, a groundbreaking peptide drug designed to prevent chemotherapy-induced peripheral neuropathy (CIPN) in breast cancer patients.

Collaborative Clinical Trial

The funding will facilitate a collaborative clinical trial led by Dr. Patrick Dillon at the University of Virginia. The trial aims to evaluate the efficacy of SP16-3M in:

– Protecting nerves from chemotherapy-induced toxicity

– Facilitating nerve repair

– Alleviating pain for breast cancer patients undergoing treatment

Addressing a Critical Need

CIPN is a common and often debilitating side effect of cancer treatment that can significantly impact patients’ quality of life. SP163M represents a potential breakthrough in managing this condition. By preventing neuropathy, SP163M could enable patients to complete their full chemotherapy regimens without dose reductions, potentially improving overall cancer treatment outcomes.

Expert Insights

Dr. Patrick Dillon expressed his enthusiasm for the collaboration: “I am excited about this partnership, as both UVA and Serpin are dedicated to finding solutions for treatment-induced neuropathy in cancer patients.”

Dr. Cohava Gelber, Founder and CEO of Serpin Pharma, also shared her thoughts: “We are thrilled to work with Dr. Dillon and UVA to bring the promise of our groundbreaking drug to breast cancer patients, aiming to prevent their suffering from debilitating pain after chemotherapy.”

Looking Ahead
The NCI award highlights the significant potential of SP163M in addressing a critical unmet need in cancer care. As Serpin Pharma advances its clinical development efforts, breast cancer patients may soon have access to this innovative therapy, enhancing their quality of life during and after chemotherapy.

 

Learn more here.

Recent News

08/25/2026

United Therapeutics Corporation Announces FDA Filing Acceptance of New Drug Application for Ralinepag to Treat Pulmonary Arterial Hypertension

United Therapeutics Corporation (Nasdaq: UTHR), a public benefit corporation, today announced that the FDA has accepted the New Drug Application (NDA) for ralinepag to treat PAH. The FDA has set a Prescription Drug User Fee Act target action date of June 24, 2027. Ralinepag has not been approved for use in any indication by the

08/19/2026

ATCC Receives New CDC Award to Advance Influenza Testing and Surveillance

ATCC has been selected by the Centers for Disease Control and Prevention (CDC) for a new contract to support serological assays for the detection and characterization of influenza viruses. The award, valued at up to $7.3 million over the 5-year contract period (contract 75D30126C21030), will support CDC’s National Center for Immunization and Respiratory Diseases, Influenza

08/18/2026

Nanochon Receives Regulatory Approval from Panamá’s Ministry of Health to Initiate First-in-Human Clinical Study of Chondrograft™

Nanochon, a medical device company developing Chondrograft™, a novel patented implant for the treatment of articular cartilage defects of the knee, today announced that it has received regulatory approval from Panamá’s Ministry of Health to initiate its First-in-Human (FIH) clinical study in Panamá. The study will evaluate the safety and performance of Chondrograft™ in patients