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Recruiting Phase 2 NCT07283692

NCT07283692 Neoadjuvant Serplulimab Plus Weekly Paclitaxel and Carboplatin in TNBC (Neo-SERPENT)

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Clinical Trial Summary
NCT ID NCT07283692
Status Recruiting
Phase Phase 2
Sponsor RenJi Hospital
Condition Triple Negative Breast Cancer
Study Type INTERVENTIONAL
Enrollment 46 participants
Start Date 2026-03-01
Primary Completion 2026-12

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age 70 Years
Study Type INTERVENTIONAL
Interventions
SerplulimabPaclitaxelCarboplatin

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

In Phase 2, researchers evaluate early signs of effectiveness. You may be randomized to receive the active treatment or a comparator. Monitoring continues closely.

This trial targets 46 participants in total. It began in 2026-03-01 with a primary completion date of 2026-12.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This is an prospective, open label, multicenter study to evaluate the efficacy and safety of neoadjuvant serplulimab plus weekly paclitaxel and carboplatin in patients with triple-negative breast cancer.

Eligibility Criteria

Inclusion Criteria: * Female, Aged ≥18 and ≤70 years * Histologically confirmed triple negative breast cancer (ER\<10%, PR\<10%, and HER2 negative) * Subjects with at least one evaluable lesion * ECOG 0-1 * Adequate organ function Exclusion Criteria: * Metastatic disease (Stage IV) * Female patients who are pregnancy, lactation or women who are of childbearing potential tested positive in baseline pregnancy test;Female patients of childbearing age that are reluctant to take effective contraceptive measures throughout the trial period

Contact & Investigator

Central Contact

Wenjin Yin, M.D.

✉ yinwenjin@renji.com

📞 86(21)68385569

Principal Investigator

Wenjin Yin, M.D.

PRINCIPAL INVESTIGATOR

Renji Hospital,School of Medicine, Shanghai Jiaotong University

Frequently Asked Questions

Who can join the NCT07283692 clinical trial?

This trial is open to female participants only, aged 18 Years or older, up to 70 Years, studying Triple Negative Breast Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

What phase is the NCT07283692 trial and what does that mean for participants?

Phase 2 trials evaluate whether the treatment shows signs of effectiveness while continuing to monitor safety. More participants are enrolled than in Phase 1 to help refine the treatment protocol.

Is NCT07283692 currently recruiting?

Yes, NCT07283692 is actively recruiting participants. Contact the research team at yinwenjin@renji.com for enrollment information.

Where is the NCT07283692 trial being conducted?

This trial is being conducted at Shanghai, China.

Who is sponsoring the NCT07283692 clinical trial?

NCT07283692 is sponsored by RenJi Hospital. The principal investigator is Wenjin Yin, M.D. at Renji Hospital,School of Medicine, Shanghai Jiaotong University. The trial plans to enroll 46 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology