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NCT05633654: Phase 3: (ASCENT-05/AFT-65 OptimICE-RD/GBG 119/NSABP B-63) Sacituzumab Govitecan-hziy and Pembrolizumab Versus Treatment of Physician's Choice in Patients With TNBC

  • CTD
  • Dec 1, 2022
  • 1 min read

Updated: 4 days ago

ascent 05

First Posted

2022-11-21

Trial status

Recruiting

Sponsor

Gilead Sciences

Abstract Presentation


Peer-reviewed journal publication


Press Release


FDA


NCCN



NCT05633654: Phase 3: (ASCENT-05/​AFT-65 OptimICE-RD/​GBG 119/​NSABP B-63) Sacituzumab Govitecan-hziy and Pembrolizumab Versus Treatment of Physician's Choice in Patients With TNBC


(Study of Sacituzumab Govitecan-hziy and Pembrolizumab Versus Treatment of Physician's Choice in Patients With Triple Negative Breast Cancer Who Have Residual Invasive Disease After Surgery and Neoadjuvant Therapy (ASCENT-05/​AFT-65 OptimICE-RD/​GBG 119/​NSABP B-63))

Official Title:

A Randomized, Open-label, Phase 3 Study of Adjuvant Sacituzumab Govitecan and Pembrolizumab Versus Treatment of Physician's Choice in Patients With Triple Negative Breast Cancer Who Have Residual Invasive Disease After Surgery and Neoadjuvant Therapy

Intervention / Treatment:

Drug: Sacituzumab govitecan-hziy (SG)

Drug: Pembrolizumab

Drug: Capecitabine

Other Study ID Numbers:

GS-US-595-6184

2024-512279-10 ( Other Identifier ) (OTHER: European Medicines Agency)


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