sac-TMT PDUFA date: FDA decision expected June 15, 2027
The FDA is expected to decide on sac-TMT from MERCK in Endometrial cancer in adult patients previously treated with platinum-containing chemotherapy and a PD-1/PD-L1 inhibitor by the PDUFA target action date of June 15, 2027. For Endometrial cancer in adult patients previously treated with platinum-containing chemotherapy and a PD-1/PD-L1 inhibitor. BLA filing. Extracted from SEC filing: EXHIBIT 99.1
A PDUFA date is the FDA's target deadline to complete its review of a drug application — approval, a complete response letter (CRL), or an extension are all possible. What is a PDUFA date? This page is research information, not financial advice.
Source: sec.gov · Data checked October 29, 2026. How we check dates. Confirm dates against the company's or the FDA's announcement before acting.
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Questions about this FDA decision
- When is the PDUFA date for sac-TMT?
- The FDA's PDUFA target action date for sac-TMT is June 15, 2027. The FDA can act before that date, and the review can be extended.
- What is sac-TMT being reviewed for?
- The application under FDA review covers Endometrial cancer in adult patients previously treated with platinum-containing chemotherapy and a PD-1/PD-L1 inhibitor.
- Which company is developing sac-TMT?
- MERCK (MRK).
- What can happen on a PDUFA date?
- The FDA approves the application, issues a complete response letter (CRL) listing what must be fixed before approval, or extends the review (typically by three months after a major amendment).