BENITIONSClinical Trial Intelligence

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

Фаза 1 Завершено NCT03239145

ЗаболеваниеAdvanced Solid Tumor
ФазаФаза 1
СпонсорDana-Farber Cancer Institute
СтатусЗавершено
Участники62 участн.
ВмешательствоPembrolizumab, Trebananib
Дата начала1.05.2018
Дата завершения13.12.2024
Публикация результатов12.03.2026

Кратко

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

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