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OncoMatch/Clinical Trials/NCT05760378

Famitinib in Combination With Camrelizumab and TPC in The First-line Treatment of Immunomodulatory Locally Advanced or Metastatic TNBC.

Is NCT05760378 recruiting? Yes, currently enrolling (Jun 2026). This Phase 3 trial studies multiple treatments including Famitinib and Camrelizumab for triple-negative breast cancer.

Phase 3RecruitingFudan UniversityNCT05760378Data as of Jun 2026Location: China

Treatment: Famitinib · Camrelizumab · nab-Palitaxel/Capecitabine/Eribulin Mesylate/CarboplatinThe study is being conducted to evaluate the Famitinib with Camrelizumab plus treatment of physician's choice (TPC) versus Camrelizumab plus TPC in Patients with Unresectable Locally Advanced or Metastatic Immunomodulatory Triple Negative Breast Cancer.

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Extracted eligibility criteria

Treatments studied

Immunotherapy

Camrelizumab

Targeted therapy

Famitinib

Chemotherapy

nab-Palitaxel/Capecitabine/Eribulin Mesylate/Carboplatin

Cancer type

Triple-Negative Breast Cancer

Breast Carcinoma

Biomarker criteria

Required: HER2 (ERBB2) wild-type

Required: ESR1 wild-type

Required: PR (PGR) wild-type

Disease stage

Required: Stage IV, III

Metastatic disease required

Cancer stage: recurrent or metastatic breast cancer; Local recurrence be confirmed by the researchers could not be radical resection.

Performance status

ECOG 0–1(Restricted strenuous activity)

Demographics

Ages ≤ 70
Female only

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Cannot have received: VEGFR inhibitor (famitinib, sorafenib, sunitinib, regorafenib)

Previous received anti-VEGFR small molecule tyrosine kinase inhibitors (e.g. famitinib, sorafenib, Sunitinib, regorafenib, etc.) for treatment of the patients

Lab requirements

Blood counts

Adequate hematologic function, laboratory test results.

Kidney function

Adequate end-organ function, laboratory test results.

Liver function

Adequate end-organ function, laboratory test results.

Adequate hematologic and end-organ function, laboratory test results.

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT05760378 currently recruiting?

Yes, this trial is currently recruiting patients.

Can patients have received prior systemic therapy?

No. This trial requires treatment-naive patients — prior systemic therapy is an exclusion criterion.

Does this trial require ERBB2?

Yes, ERBB2 wild-type is a required biomarker for enrollment.

Does this trial require ESR1?

Yes, ESR1 wild-type is a required biomarker for enrollment.

Does this trial require PGR?

Yes, PGR wild-type is a required biomarker for enrollment.

What disease stage is eligible?

Stage IV or III is required (metastatic disease required).

Is there an age limit?

Yes. Patients must be 70 years or younger.

Is this trial open to male patients?

No. This trial enrolls female patients only.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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