Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**Acapatamab + AMG 404** is an investigational combination therapy studied primarily for metastatic castration-resistant prostate cancer (mCRPC). **Acapatamab** (AMG 160) is a half-life extended bispecific T-cell engager (BiTE) that targets prostate-specific membrane antigen (PSMA) on tumor cells and CD3 on T cells, promoting immune-mediated killing of prostate cancer cells. **AMG 404** is a monoclonal antibody targeting programmed cell death protein 1 (PD-1), functioning as a checkpoint inhibitor to enhance T-cell anti-tumor activities. This combination aims to leverage direct T-cell-mediated cytotoxicity against PSMA-positive tumor cells (acapatamab) while overcoming checkpoint-mediated immunosuppression (AMG 404). Early-phase clinical trials have demonstrated manageable safety profiles, notable cytokine release syndrome, and preliminary anti-tumor activity, but no approvals as of now[2][3][5][7].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on acapatamab + AMG 404.