FUSCC Refractory TNBC Platform Study (FUTURE2.0)

NCT05749588 · Status: RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2026-04-16

No results posted yet for this study

Summary

This is a Phase II, open-label, Single-center platform study research based on molecular subtypes to explore precision therapy in refractory triple-negative breast cancer.

Conditions

  • Triple-negative Breast Cancer

Interventions

DRUG

A1: SHR-A1811

A1: an anti-HER2 antibody-drug conjugate (ADC)

DRUG

A2: SHR-A1811 with Camrelizumab with famitinib

A2: SHR-A1811: an anti-HER2 antibody-drug conjugate (ADC) Camrelizumab: an anti-programmed death-1 (PD-1) antibody

DRUG

B1: TROP2 ADC

B1: an Trophoblast cell-surface antigen 2 (TROP2) ADC

DRUG

B2: TROP2 ADC with Camrelizumab

B2: TROP2 ADC : an Trophoblast cell-surface antigen 2 (TROP2) ADC Camrelizumab: an anti-programmed death-1 (PD-1) antibody

DRUG

C1: SHR-A1811

C1: an anti-HER2 antibody-drug conjugate (ADC)

DRUG

C2: SHR-A1811 with BP102

C2: SHR-A1811: an anti-HER2 antibody-drug conjugate (ADC) BP102: a humanized recombinant monoclonal IgG1 antibody (biosimilar to bevacizumab)

DRUG

D1: TROP2 ADC

D1: an Trophoblast cell-surface antigen 2 (TROP2) ADC

DRUG

D2: TROP2 ADC with BP102

D2: TROP2 ADC : an Trophoblast cell-surface antigen 2 (TROP2) ADC BP102: a humanized recombinant monoclonal IgG1 antibody (biosimilar to bevacizumab)

DRUG

E1: SHR-A1811

E1: an anti-HER2 antibody-drug conjugate (ADC)

DRUG

F1: TROP2 ADC

F1: an Trophoblast cell-surface antigen 2 (TROP2) ADC

DRUG

G1: SHR-A1811

G1: an anti-HER2 antibody-drug conjugate (ADC)

DRUG

H1: TROP2 ADC

H1: an Trophoblast cell-surface antigen 2 (TROP2) ADC

DRUG

E2: SHR-A1811 with everolimus

E1: SHR-A1811 an anti-HER2 antibody-drug conjugate (ADC) everolimus: an mTOR inhibitor

DRUG

TQB2102 with TQB2868

TQB2102: an anti-HER2 antibody-drug conjugate (ADC) TQB2868: an anti-PD-1/TGF-β bispecific antibody in all-comer TNBC

Sponsors & Collaborators

  • Fudan University

    lead OTHER

Principal Investigators

  • Zhimin Shao, M.D. · Fudan University

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-03-30
Primary Completion
2027-12-31
Completion
2028-12-31

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05749588 on ClinicalTrials.gov