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DRUG CLASS:

PD1 inhibitor

Related drugs:
20h
New P2 trial
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Lenvima (lenvatinib) • Qibeian (iparomlimab/tuvonralimab)
21h
CA209-9WW: Nivolumab or Nivolumab and Azacitidine in Patients With Recurrent, Resectable Osteosarcoma (clinicaltrials.gov)
P1, N=21, Active, not recruiting, H. Lee Moffitt Cancer Center and Research Institute | Trial completion date: Dec 2025 --> Apr 2026
Trial completion date
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Opdivo (nivolumab) • azacitidine
21h
Neo ReNi II: A Phase 2 Clinical Trial of Neoadjuvant Relatlimab and Nivolumab in High Risk, Clinical Stage II Cutaneous Melanoma (clinicaltrials.gov)
P2, N=20, Active, not recruiting, Melanoma Institute Australia | Trial completion date: Jan 2036 --> Oct 2035
Trial completion date
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BRAF (B-raf proto-oncogene)
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BRAF mutation • NRAS mutation • NRAS wild-type
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Opdualag (nivolumab/relatlimab-rmbw)
21h
Adaptive BRAF-MEK Inhibitor Therapy for Advanced BRAF Mutant Melanoma (clinicaltrials.gov)
P1, N=14, Active, not recruiting, H. Lee Moffitt Cancer Center and Research Institute | Trial completion date: Dec 2028 --> Dec 2026
Trial completion date
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BRAF V600E • BRAF V600
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Opdivo (nivolumab) • Mektovi (binimetinib) • Braftovi (encorafenib)
23h
Phase I Open-Label Safety Trial of Pembrolizumab for Neurological Post- Acute Sequelae of SARS-CoV-2 (PD1-PASC I) (clinicaltrials.gov)
P1, N=15, Not yet recruiting, National Institute of Neurological Disorders and Stroke (NINDS)
New P1 trial • IO biomarker
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CD8 (cluster of differentiation 8) • PD-1 (Programmed cell death 1)
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Keytruda (pembrolizumab)
23h
New P1 trial
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Tevimbra (tislelizumab-jsgr) • triptorelin • goserelin acetate
24h
LIBRA: A Study of Novel Combinations in Non-Small Cell Lung Cancer (NSCLC) (clinicaltrials.gov)
P2, N=278, Recruiting, AstraZeneca | Trial primary completion date: Mar 2027 --> Apr 2029
Trial primary completion date
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EGFR (Epidermal growth factor receptor) • PD-L1 (Programmed death ligand 1) • ALK (Anaplastic lymphoma kinase)
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ALK rearrangement
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Cyramza (ramucirumab) • Datroway (datopotamab deruxtecan-dlnk) • rilvegostomig (AZD2936)
24h
Phase II Trial of the PARP Inhibitor Niraparib and PD-1 Inhibitor Dostarlimab in Patients With Advanced Cancers With Active Progressing Brain Metastases (STARLET) (clinicaltrials.gov)
P2, N=120, Recruiting, M.D. Anderson Cancer Center | Trial completion date: Feb 2026 --> Dec 2029 | Trial primary completion date: Feb 2026 --> Dec 2029
Trial completion date • Trial primary completion date
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PD-L1 (Programmed death ligand 1) • HRD (Homologous Recombination Deficiency) • CDK12 (Cyclin dependent kinase 12) • CHEK2 (Checkpoint kinase 2) • RAD51 (RAD51 Homolog A) • RAD51B (RAD51 Paralog B) • BRIP1 (BRCA1 Interacting Protein C-terminal Helicase 1) • RAD51C (RAD51 paralog C) • RAD51D (RAD51 paralog D) • CHEK1 (Checkpoint kinase 1) • RAD54L (DNA Repair And Recombination Protein RAD54) • FANCL (FA Complementation Group L) • RAD52 (RAD52 Homolog DNA Repair Protein)
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PD-L1 expression
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Zejula (niraparib) • Jemperli (dostarlimab-gxly)
1d
BBOpCo: Botensilimab and Balstilimab Optimization in Colorectal Cancer (clinicaltrials.gov)
P2, N=16, Active, not recruiting, Nicholas DeVito, MD | Recruiting --> Active, not recruiting
Enrollment closed
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MSI (Microsatellite instability)
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MSI-H/dMMR
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Avastin (bevacizumab) • 5-fluorouracil • Vectibix (panitumumab) • oxaliplatin • leucovorin calcium • balstilimab (AGEN2034) • botensilimab (AGEN1181)
1d
Perioperative Enfortumab Vedotin (EV) Plus Pembrolizumab (MK-3475) Versus Neoadjuvant Chemotherapy for Cisplatin-Eligible Muscle Invasive Bladder Cancer (MIBC) (MK-3475-B15/ KEYNOTE-B15 / EV-304) (clinicaltrials.gov)
P3, N=808, Completed, Merck Sharp & Dohme LLC | Active, not recruiting --> Completed | Trial completion date: Dec 2026 --> Oct 2025 | Trial primary completion date: Dec 2026 --> Oct 2025
Trial completion • Trial completion date • Trial primary completion date
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Keytruda (pembrolizumab) • cisplatin • gemcitabine • Padcev (enfortumab vedotin-ejfv)
1d
Real-World Long-Term Outcomes of First-Line Pembrolizumab in Advanced PD-L1 ≥ 50% NSCLC: A Systematic Review and Meta-analysis. (PubMed, Ann Surg Oncol)
Real-world evidence confirms the long-term effectiveness and safety of pembrolizumab monotherapy for advanced NSCLC with PD-L1 ≥50%. Survival outcomes closely mirrored those from previous trials, supporting the generalizability of pembrolizumab's benefit across routine practice.
Retrospective data • Review • Journal • Real-world evidence • PD(L)-1 Biomarker • IO biomarker
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EGFR (Epidermal growth factor receptor) • PD-L1 (Programmed death ligand 1) • ALK (Anaplastic lymphoma kinase)
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PD-L1 expression
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Keytruda (pembrolizumab)
1d
JGOG3029: Assessment of the Efficacy and Safety of Pembrolizumab for Ovarian Squamous Cell Carcinoma (clinicaltrials.gov)
P2, N=21, Active, not recruiting, Niigata University Medical & Dental Hospital | Recruiting --> Active, not recruiting
Enrollment closed
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Keytruda (pembrolizumab)