FDAsafety guidance66% confidence
FDA AP — INQOVI (SUPPL)
Source: FDA
Why This Matters
Why this matters: sets a safety guidance precedent in the same sub-indication (colorectal cancer) as Roche; the same agency is already in play for this signal, so precedent weight is higher.
Regulatory Analysis
Application NDA212576. Sponsor: TAIHO ONCOLOGY. Submission status: AP. Submission type: SUPPL. Review priority: STANDARD. Active ingredients: CEDAZURIDINE, DECITABINE.
Supporting Context
- Therapeutic area
- Oncology · Immunotherapy
- Sub-indication
- Colorectal Cancer
Related signal: FDA grants Priority Review for Roche’s Tecentriq in stage III colon cancer