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ApprovalJun 12, 2026137 days ago

FDA approves KEYTRUDA with WELIREG for adjuvant clear cell renal cell carcinoma

The FDA approved Merck &’s KEYTRUDA (pembrolizumab) + WELIREG (belzutifan) for Adjuvant clear cell renal cell carcinoma on Jun 12, 2026. The company can now sell it in that market.

Plain-English summary generated from this entry’s own fields (drug, condition, stage, date). Glossary

DetailsRegulatory approval
Company
Merck & Co., Inc. MRK
Drug
KEYTRUDA (pembrolizumab) + WELIREG (belzutifan)
For
Adjuvant clear cell renal cell carcinoma
Stage
Regulatory (sBLA)
When
Jun 12, 2026
Source note
First approved PD-1 plus HIF-2alpha inhibitor combination, cleared for adjuvant treatment of ccRCC patients at intermediate-high or high risk of recurrence after nephrectomy.
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Merck & Co., Inc.
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Drug
sacituzumab tirumotecan (MK-2870)
For
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Stage
Phase 3 · the last stage before a drug can be approved
When
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Source note
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Plain-English summary generated from this entry’s own fields (drug, condition, stage, date). Glossary · Open this catalyst’s page