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Clinical trial intelligence report
A Phase 1b Study of BCL-XL Degrader DT2216 in Combination With Weekly Paclitaxel in Recurrent Platinum-resistant Ovarian Cancer
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Aug 04, 2026
Report code
NCT06964009-Aug 04, 2026
NCT ID
NCT06964009
Status
RECRUITING
Phase
Phase 1b
Sponsor
Elizabeth Stover, MD, PhD
Executive brief
Investment-Ready Snapshot
DT2216, a BCL-XL degrader, is being evaluated in combination with paclitaxel for recurrent platinum-resistant ovarian cancer. The study aims to establish the maximum tolerated dose (MTD) and assess safety, potentially positioning DT2216 as a novel therapeutic option in a market with limited effective treatments for this patient population. Given the high unmet need in recurrent ovarian cancer, successful outcomes could lead to significant commercial opportunities. The collaboration with Dialectic Therapeutics and funding from the Department of Defense may enhance credibility and support for further development. However, the competitive landscape includes existing therapies and ongoing trials targeting similar pathways, necessitating diligent monitoring of competitor advancements and regulatory pathways.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT06964009
Indication
Ovarian Cancer
Modality
small molecule
Target
BCL-XL protein (degradation via proteolysis-targeting chimera, PROTAC mechanism)
Intervention
DT2216, Paclitaxel
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.