RecruitingPhase 1NCT06964009

DT2216 + Paclitaxel in Platinum-Resistant Ovarian Cancer

A Phase 1b Study of BCL-XL Degrader DT2216 in Combination With Weekly Paclitaxel in Recurrent Platinum-resistant Ovarian Cancer


Sponsor

Elizabeth Stover, MD, PhD

Enrollment

30 participants

Start Date

Sep 22, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this research study is determining the highest dose of the study drug DT2216 in combination with paclitaxel that can be safely and tolerably administered in recurrent ovarian cancer. The names of the study drugs involved in this study are: * DT2216 (a type of proteolysis-targeting chimera degrader of BCL-XL protein) * Paclitaxel (a type of antimicrotubule agent)


Eligibility

Sex: FEMALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a new drug called DT2216 combined with paclitaxel (a standard chemotherapy) for women with ovarian, fallopian tube, or peritoneal cancer that has come back or stopped responding to platinum-based chemotherapy. **You may be eligible if...** - You have a confirmed diagnosis of recurrent or treatment-resistant ovarian, fallopian tube, or peritoneal cancer - Your cancer can be measured on a scan (at least one lesion of a specific size) - You have adequate organ function to tolerate treatment **You may NOT be eligible if...** - Your cancer has not previously been treated with platinum-based chemotherapy - You have significant heart, kidney, or liver problems - You are pregnant or breastfeeding - You have had certain recent surgeries or other investigational treatments Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGDT2216

A proteolysis-targeting chimera (PROTAC) degrader, single-use vial, via intravenous (into the vein) infusion.

DRUGPaclitaxel

An antimicrotubule agent, multi-dose vial, via intravenous (into the vein) infusion per institutional standard.


Locations(3)

Beth Israel Deaconess Medical Center (BIDMC)

Boston, Massachusetts, United States

Dana Farber Cancer Institute

Boston, Massachusetts, United States

Brigham and Women's Hospital

Boston, Massachusetts, United States

View Full Details on ClinicalTrials.gov

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NCT06964009


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