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anti-b7-h3 antibody-drug conjugate db-1311

Generic: Anti-B7-H3 Antibody-drug Conjugate DB-1311

anti-b7-h3 antibody-drug conjugate db-1311: 3 clinical trials tracked.

anti-b7-h3 antibody-drug conjugate db-1311 evidence translation

What we can confirm

3 tracked trials

No verified listed company relationship

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about anti-b7-h3 antibody-drug conjugate db-1311, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence2 indications · 1 study sponsors
Clinical Trial Registry Records (3)

A Phase III, Randomized, Open-label Trial of BNT324 Versus Docetaxel With Prednisone/Prednisolone in Metastatic Castration-resistant Prostate Cancer

NCT07365995Registry updated 2026-09-18·Phase 3·BNTX
Recruiting

Primary endpoint: rPFS assessed by BICR

InterventionalRandomizedopen736 targetStarted 2026-04Completion 2031-0233 sites · Australia, China, United Kingdom, United StatesBioNTech SE

A Phase Ib/II, Multi-site, Open-label, Two-part Trial to Evaluate the Efficacy, Safety, Pharmacokinetics, and Recommended Combination Dose of BNT324 With BNT327 in Participants With Advanced Lung Cancer

NCT06892548Registry updated 2026-08-26·Phase 1/Phase 2·BNTX
Recruiting

Primary endpoint: Part 1 - Occurrence of dose limiting toxicities (DLTs) by dose level

InterventionalRandomizedopen594 targetStarted 2025-05Completion 2032-0550 sites · Australia, China, United StatesBioNTech SE

A Phase 1/2a, Multicenter, Open-Label, First in Human Study to Assess the Safety, Tolerability, Pharmacokinetics, and Preliminary Antitumor Activity of DB-1311 in Subjects With Advanced/Metastatic Solid Tumors

NCT05914116Registry updated 2025-11-21·Phase 1
Recruiting

Primary endpoint: Phase 1: Percentage of Participants with Dose-Limiting Toxicities (DLTs) as assessed by Common Terminology Criteria for Adverse Events (CTCAE) v5.0. Percentage of participants in Part 1 with DLTs

Interventionalopen862 targetStarted 2023-08Completion 2028-0550 sites · Australia, China, United StatesDualityBio Inc.