- BNT324/DB-1311 showed encouraging antitumor activity and a manageable safety profile in a Phase 1/2a clinical trial in heavily pretreated patients with locally advanced or metastatic solid tumors, including small cell lung cancer ("SCLC"), non-small cell lung cancer ("NSCLC"), and castration-resistant prostate cancer ("CRPC").
- In patients with SCLC with at least one post-baseline tumor assessment and who had received prior immunotherapy but no prior topoisomerase 1 inhibitor, the unconfirmed objective response rate ("uORR") was 70.4% at the BNT324/DB-1311 9 mg/kg dose level.
- In patients with CRPC, the uORR was 28.0%; imaging progression-free survival ("rPFS") data are not yet mature, with a median rPFS of 7.2 months and a 6-month rPFS rate of 94.7%.
- Multiple clinical trials combining selected assets from BioNTech's and DualityBio's strategic partnership with BNT327/PM8002, an investigational bispecific antibody targeting PD-L1 and VEGF-A, are planned; a Phase 1/2 trial evaluating BNT324/DB-1311 with BNT327/PM8002 in patients with SCLC or NSCLC is planned to start in 2025.
Reported Earlier, Duality Biologics And BioNtech Reveals Interim Results For B7-H3 Antibody-Drug Conjugate BNT324/DB-1311 In Advanced Solid Tumors At ESMO Asia Congress 2024
The above content is for informational or educational purposes only and does not constitute any investment advice related to Futu. Although we strive to ensure the truthfulness, accuracy, and originality of all such content, we cannot guarantee it.
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