REM-001
Phase 2- Indications
- Cutaneous metastatic breast cancer, Recurrent basal cell carcinoma, Nevus syndrome
Company intelligence / Profile preview
REM‑001 has demonstrated an approximately 80% complete response rate in evaluable cutaneous metastatic breast cancer lesions across multiple late-stage trials. The safety database includes nearly 1,100 patients across various indications. Current open-label studies are ongoing to optimize dosing and support future Phase III development. NIH SBIR funding supports the current trial. FDA fast track designation granted for REM‑001 in CMBC.
1 more asset in the full pipeline.
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