BENITIONSClinical Trial Intelligence

Pembrolizumab (Anti-PD-1) and AMG386 (Angiopoietin-2 (Ang-2) in Patients With Advanced Solid Tumor

Phase 1 Completed NCT03239145

ConditionAdvanced Solid Tumor
PhasePhase 1
SponsorDana-Farber Cancer Institute
StatusCompleted
Enrollment62 participants
InterventionsPembrolizumab, Trebananib
Start dateMay 1, 2018
Completion dateDec 13, 2024
Results postedMar 12, 2026

Summary

This research study is studying an investigational combination of drugs as a possible treatment for advanced solid tumors: melanoma, ovarian, renal, or colorectal cancer. The drugs involved in this study are: * Pembrolizumab * AMG386

Number of Participants Experienced Dose Limit Toxicities (DLT)

3 weeks · Participants

[Dose Escalation Dose Level I] Pembrolizumab + Trebananib0 Participants
[Dose Escalation Dose Level II] Pembrolizumab + Trebananib0 Participants

Maximum Tolerated Dose (MTD) of Trebananib

3 weeks · mg/kg

[Dose Escalation Dose Level I and Dose Level II] Pembrolizumab + Trebananib30 mg/kg

Grade 3 or Higher Toxicity Rate in Expansion Cohort

The median follow up time was 3.3 months (range: 0.6 to 25.3 months). · percentage of participants

[Dose Expansion Dose Level II] Pembrolizumab + Trebananib (Colorectal)59.5 percentage of participants
Dose Expansion Dose Level II] Pembrolizumab + Trebananib (Ovarian)63.6 percentage of participants
Dose Expansion Dose Level II] Pembrolizumab + Trebananib (Renal Cell Carcinoma)75.0 percentage of participants

Open in BENITIONS View on ClinicalTrials.gov

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