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FDA Grants Fast Track Status to OnCusp's Novel Antibody-Drug Conjugate for Platinum-Resistant Ovarian Cancer

7 months ago2 min read

Key Insights

  • The FDA has awarded Fast Track Designation to CUSP06, an innovative Cadherin-6 targeting Antibody-Drug Conjugate developed by OnCusp Therapeutics for platinum-resistant ovarian cancer treatment.

  • Early Phase 1 trial results demonstrate promising anti-tumor activity and manageable safety profile for CUSP06 in patients with platinum-refractory/resistant ovarian cancer.

  • This regulatory milestone will accelerate the development process, potentially bringing a new therapeutic option to an underserved patient population more quickly.

OnCusp Therapeutics announced today that its lead program CUSP06, a novel Cadherin-6 targeting Antibody-Drug Conjugate (CDH6 ADC), has received Fast Track Designation from the U.S. Food and Drug Administration for treating patients with platinum-resistant ovarian cancer (PROC).
The regulatory milestone marks a significant step forward in addressing the urgent need for new treatment options in this challenging disease setting. Fast Track Designation is designed to facilitate the development and expedite the review of drugs that treat serious conditions and fill unmet medical needs.
"We are extremely pleased that the FDA granted Fast Track Designation to CUSP06," said Eric Slosberg, PhD, Chief Development Officer of OnCusp Therapeutics. "The early results from our Phase 1 trial have been encouraging, and this designation will expedite our efforts to bring this potentially transformative therapy to patients."

Clinical Development Progress

The ongoing Phase 1 multicenter study (CUSP06-1001) is evaluating CUSP06 in adult patients with platinum-refractory/resistant ovarian cancer and other advanced solid tumors. The trial's primary objectives include assessing the safety and tolerability of the drug, while also examining its pharmacokinetic properties and preliminary efficacy signals.
Initial data from the trial has yielded promising results, with investigators observing encouraging anti-tumor effects coupled with a manageable safety profile. These findings support the continued development of the program and suggest potential therapeutic value for patients with limited treatment options.

Addressing an Unmet Medical Need

Platinum-resistant ovarian cancer represents a significant therapeutic challenge in oncology. Patients whose disease progresses during or shortly after platinum-based chemotherapy typically face poor prognoses and limited treatment alternatives. The development of CUSP06, with its targeted approach using antibody-drug conjugate technology, could potentially offer a new therapeutic strategy for this underserved patient population.
Dr. Slosberg emphasized the company's commitment to accelerated development, stating, "Given the need for new therapeutic options in this underserved population, we are committed to working closely with the FDA to accelerate its development."

Therapeutic Approach

CUSP06's mechanism of action, targeting Cadherin-6 through an antibody-drug conjugate platform, represents a novel approach in ovarian cancer treatment. This precision medicine strategy aims to deliver potent anti-cancer agents specifically to tumor cells while potentially minimizing effects on healthy tissue.
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