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Therapeutic Area

PD-1 Inhibitor

Therapeutic area intelligence for PD-1 Inhibitor with 10 indexed intelligence signals across regulatory, clinical, competitive, and market developments.

Signals
10
Catalysts
0
Companies
2

Companies

Bristol Myers Squibb →
Merck →

Assets

FDA →
KEYTRUDA →
Oncology →
OPDIVO →
pembrolizumab →
Tislelizumab →

Recent signals(10)

ClinicalJuly 18, 2026

Merck's Pembrolizumab Study Targets Japanese Pediatric and Adult Cancer Patients

Merck is conducting a study to evaluate the safety and efficacy of pembrolizumab in Japanese pediatric participants with solid tumors and lymphomas, as well as in adults with Merkel cell carcinoma.

RegulatoryJuly 15, 2026

FDA Grants Priority Review for KEYTRUDA QLEX Supplement Application

The FDA has accepted the supplemental application for KEYTRUDA QLEX, indicating a priority review status.

RegulatoryJuly 15, 2026

FDA grants priority review for KEYTRUDA supplemental application

The FDA has granted priority review for the supplemental application of KEYTRUDA (pembrolizumab) submitted by Merck Sharp & Dohme.

RegulatoryJuly 15, 2026

FDA Grants Priority Review for KEYTRUDA QLEX Supplement Application

The FDA has granted priority review for the supplemental application of KEYTRUDA QLEX, which includes pembrolizumab and berahyaluronidase alfa-PMPH.

RegulatoryJuly 15, 2026

FDA Submission Update for KEYTRUDA (Pembrolizumab) by Merck

Merck Sharp Dohme has submitted a supplemental application for KEYTRUDA (pembrolizumab) under BLA125514.

RegulatoryJuly 15, 2026

FDA Accepts Supplement Application for OPDIVO (Nivolumab) by Bristol Myers Squibb

The FDA has accepted a supplemental application for OPDIVO (Nivolumab) from Bristol Myers Squibb.

ClinicalJuly 12, 2026

Phase 2 Study of Tislelizumab in MSI-H or dMMR Solid Tumors by BeiGene

A Phase 2 study is underway evaluating Tislelizumab in patients with MSI-H or dMMR solid tumors.

RegulatoryJune 30, 2026

FDA Accepts Supplemental Application for KEYTRUDA QLEX

The FDA has accepted a supplemental application for KEYTRUDA QLEX, which includes pembrolizumab and berahyaluronidase alfa-PMPH.

RegulatoryJune 30, 2026

FDA Approves Supplement for KEYTRUDA (pembrolizumab) by Merck

The FDA has approved a supplemental application for KEYTRUDA (pembrolizumab) from Merck.

RegulatoryJune 18, 2026

FDA Grants Priority Review for KEYTRUDA QLEX Supplement Application

The FDA has granted priority review for the supplemental application of KEYTRUDA QLEX, which includes pembrolizumab and berahyaluronidase alfa-PMPH.

Upcoming catalysts

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Indications

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