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NCT05088057

Neoadjuvant Camrelizumab Plus Chemotherapy in Triple Negative Breast Cancer

Status unknown Phase 2 Last updated 21 October 2021
What this trial tests

Phase 2 trial testing Camrelizumab in Triple Negative Breast Cancer (TNBC) in 30 participants. Status unknown.

Timeline
20 September 2021
Primary endpoint
19 August 2024
1 November 2024

Quick facts

Lead sponsorAiping Shi
PhasePhase 2
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment30
Start date20 September 2021
Primary completion19 August 2024
Estimated completion1 November 2024
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Aiping Shi

Who can join

Adults 18 to 70, female only, with Triple Negative Breast Cancer (TNBC). Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to evaluate the efficacy and safety of Camrelizumab plus chemotherapy as neoadjuvant therapy and Camrelizumab as adjuvant therapy in participants who have triple negative breast cancer (TNBC).

Publications & conference data

3 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Research progress on immunotherapy in triple‑negative breast cancer (Review).
    Zhang X, Ge X, Jiang T, Yang R, et al · · 2022 · cited 20× · PMID 35762339 · DOI 10.3892/ijo.2022.5385
  2. Evolving treatment landscape of immunotherapy in breast cancer: current issues and future perspectives.
    Valenza C, Rizzo G, Passalacqua MI, Boldrini L, et al · · 2023 · cited 10× · PMID 36743524 · DOI 10.1177/17588359221146129
  3. Immunotherapy and its racial specificity for breast cancer treatment in Asia: a narrative review.
    Xu RC, Zhang YW, Liu CC, Xu YY, et al · · 2025 · cited 3× · PMID 40443538 · DOI 10.1016/j.lanwpc.2024.101180

Verify or expand the search:

Other trials of Camrelizumab

Trials testing the same drug.

Other recruiting trials for Triple Negative Breast Cancer (TNBC)

Currently open trials in the same condition.

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Data sources for this page

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