Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06636981

All Trans Retinoic Acid Combined with Toripalimab+Chemotherapy for Locally Advanced Inoperable or Metastatic Triple Negative Breast Cancer:a Multi-center, Multi-cohort Phase II Trial

Status
Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
129 (estimated)
Sponsor
Fudan University · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

All trans retinoic acid Combined with Toripalimab+Chemotherapy for Locally Advanced inoperable or Metastatic Triple Negative Breast Cancer:a multi-center, multi-cohort phase II trial

Conditions

Interventions

TypeNameDescription
DRUGCohort2: ATRA+Toripalimab+TPCReceive 200 mg D1 of Toripalimab via intravenous infusion for a course of 21 days; TPC regimen (monoclonal antibody 10mg/kg D1, 8 intravenous infusions, 1 course of treatment every 21 days; Elibulin 1.4mg/m2 D1, 8 intravenous infusions, 1 course of treatment every 21 days; Utideron 40mg/m2 D1-5 intravenous infusions, 1 course of treatment every 21 days; Gemcitabine 1000mg/m2 D1, 8 intravenous infusions, 1 course of treatment every 21 days; Albumin paclitaxel 100 mg/m2 D1, D8, intravenous infusion, 1 course of treatment every 21 days); Capecitabine 1000mg/m2, D1-14, oral, one course of treatment every 21 days); All trans retinoic acid 20 mg bid, orally, D-3-D11, administered continuously for 14 days, stopped for 7 days, with one course of treatment lasting 21 days.
DRUGCohort1: ATRA+Toripalimab+chemoReceive 200 mg of Toripalimab via D1 intravenous infusion, with 21 days as one course of treatment; Albumin paclitaxel 100 mg/m2, D1, D8, intravenous infusion, one course of treatment for 21 days; All trans retinoic acid 20 mg bid, oral, D-3-D11, continuous administration for 14 days, cessation for 7 days, 21 days is one course of treatment.

Timeline

Start date
2024-11-04
Primary completion
2029-09-01
Completion
2029-09-01
First posted
2024-10-15
Last updated
2024-12-13

Locations

2 sites across 1 country: China

Source: ClinicalTrials.gov record NCT06636981. Inclusion in this directory is not an endorsement.