A Phase Ib/II Clinical Trial to Evaluate the Safety and Efficacy of TQB2930 for Injection Monotherapy or in Combination for the Treatment of Human Epidermal Growth Factor Receptor 2 (HER2)-Positive Recurrent / Metastatic Breast Cancer

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1/Phase 2
SUMMARY

This is a phase Ib/II exploratory study. Phase Ib includes the dose escalation and expansion study of monotherapy, as well as the dose escalation study of combination therapy. After determining the maximum tolerated dose (MTD), a dose expansion study is conducted to observe the safety and efficacy in monotherapy. Phase II study is to further observe the safety and efficacy of TQB2930 combined with albumin-paclitaxel (cohort 3), or chemotherapy selected by investigators (cohort 4).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

• Age: 18-75 years old; Eastern Cooperative Oncology Group Performance Status (ECOG PS) score: 0\

∙ 1; The expected survival is over 3 months.

• Phase Ib

‣ Advanced malignancies confirmed by cytology / histopathology, priority given to subjects with HER2 expression or amplification;

⁃ Subjects with malignant tumors who have failed standard treatment or lack effective treatment;

⁃ Confirmed presence of at least one evaluable lesion according to RECIST 1.1 criteria

• Phase II

‣ Hormone receptor (HR)-negative, HER2-positive breast cancer confirmed by cytology / histopathology, with evidence of local recurrence or distant metastasis, unsuitable for surgery or radiotherapy for curative purposes:

⁃ Have not received systemic antitumor therapy for metastatic stage; Systemic use of endocrine therapy is permitted, but not exceed 2 lines;

⁃ at least one measurable lesion that meets the RECIST 1.1 criteria.

• Major organs are functioning normally.

• Female subjects of reproductive age should agree to use contraceptive methods during the study period and until 6 months after the end of the study; Negative serum pregnancy / urine pregnancy test within 7 days prior to study enrollment and must be non-lactating subjects; Male subjects should agree to use contraception during the study and until six months after the end of the study.

Locations
Other Locations
China
Affiliated Cancer Hospital of Chongqing University
RECRUITING
Chongqing
Affiliated cancer hospital of harbin medical university
RECRUITING
Harbin
Contact Information
Primary
Qingyuan Zhang, Doctor
sy86298276@163.com
+86 0451 86298070
Backup
Xiaohua Zeng, Doctor
zengxiaohua000017@163.com
13983687701
Time Frame
Start Date: 2023-04-13
Estimated Completion Date: 2027-10
Participants
Target number of participants: 154
Treatments
Experimental: TQB2930 for injection
TQB2930 for injection,10 mg/kg, quaque week (QW), 21 day as a treatment cycle; TQB2930 for injection, 20 mg/kg, quaque 2 weeks (Q2W), 28 day as a treatment cycle; TQB2930 for injection,30 mg/kg, quaque 3 weeks (Q3W), 21 day as a treatment cycle.
Experimental: TQB2930 for injection 30mg/kg + Paclitaxel for injection (albumin-bound)
TQB2930 for injection 30mg/kg combined with paclitaxel (albumin-bound) for injection, 21 days for one treatment cycle
Experimental: TQB2930 for injection+TQB3616 capsule for injection + fulvestrant injection
TQB2930 for injection 20mg/kg combined with TQB3616 capsule 120mg or 150mg or 180mg, and fulvestrant injection. Q2W, 28 days a cycle.
Experimental: TQB2930 for injection + chemotherapy
TQB2930 for injection 30mg/kg combined with capecitabine tablets or vinorelbine tartrate injection or eribulin mesylate injection or gemcitabine hydrochloride for injection, 21 days a cycle.
Related Therapeutic Areas
Sponsors
Leads: Chia Tai Tianqing Pharmaceutical Group Co., Ltd.

This content was sourced from clinicaltrials.gov

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