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A Study of TQB2450 Combined With Anlotinib in Subjects With Gynecological Cancer

Sponsor
Chia Tai Tianqing Pharmaceutical Group Co., Ltd. (Industry)
Overall Status
Recruiting
CT.gov ID
NCT04236362
Collaborator
(none)
90
Enrollment
5
Locations
1
Arm
27
Anticipated Duration (Months)
18
Patients Per Site
0.7
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This is a single-arm, open-label, phase Ib clinical trial to evaluate the efficacy and safety of TQB2450 combined with anlotinib in subjects with gynecological cancer, including 34 ovarian cancer，34 endometrial cancer，22 cervical cancer.

Condition or Disease Intervention/Treatment Phase
Phase 1/Phase 2

Study Design

Study Type:
Interventional
Anticipated Enrollment :
90 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
A Phase Ib, Single Arm, Open-label Study of TQB2450 Combined With Anlotinib in Subjects With Relapsed / Refractory Gynecological Cancer
Actual Study Start Date :
Feb 27, 2020
Anticipated Primary Completion Date :
Dec 31, 2021
Anticipated Study Completion Date :
May 30, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: TQB2450+Anlotinib

TQB2450 1200 mg IV on Day 1 of each 21-day cycle plus Anlotinib capsules given orally in fasting conditions , once daily in 21-day cycle (14 days on treatment from Day 1-14, 7 days off treatment from Day 15-21)

Drug: TQB2450
TQB2450 is a humanized monoclonal antibody targeting programmed death ligand-1 (PD-L1), which prevents PD-L1 from binding to PD-1 and B7.1 receptors on T cell surface, restores T cell activity, thus enhancing immune response and has potential to treat various types of tumors.

Drug: Anlotinib
A multi-target receptor tyrosine kinase inhibitor

Outcome Measures

Primary Outcome Measures

  1. Objective Response Rate (ORR) [up to 96 weeks]

    Percentage of Participants Achieving Complete Response (CR) and Partial Response (PR)

Secondary Outcome Measures

  1. Progression free survival (PFS) [up to 96 weeks]

    PFS defined as the time from randomization until the first documented progressive disease (PD) or death from any cause.

  2. Duration of Response (DOR) [up to 96 weeks]

    Time from tumor first assessment to CR or PR to first assessment to PD (Progressive Disease) or death from any cause

  3. Disease control rate（DCR） [up to 96 weeks]

    Percentage of Participants Achieving Complete Response (CR) and Partial Response (PR) and Stable Disease (SD).

  4. Overall Survival (OS) [up to 120 weeks]

    OS defined as the time from randomization to death from any cause. Participants who do not die at the end of the extended follow-up period, or were lost to follow-up during the study, were censored at the last date they were known to be alive.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

  1. Understood and signed an informed consent form;

  2. 18 years and older, male or female, Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1, life expectancy ≥ 3 months;

  3. Histologically confirmed, unresectable recurrent/metastatic advanced gynecologic cancer, including ovarian, endometrial, and cervical cancer;

  4. Subjects have received at least 1 line platinum-containing chemotherapy (minimum of 4 cycles of platinum-containing treatment) after tumor reduction, and meet any of the following：Platinum-resistant or refractory patients, including patients who have progressed or relapsed during previous platinum-containing chemotherapy regimens or within 6 months after the end of platinum-containing chemotherapy;

  5. At least one measurable lesion according to the RECIST 1.1;

  6. The main organs function are normally;

  7. Male or female subjects should agree to use an adequate method of contraception starting with the first dose of study therapy through 6 months after the last dose of study (such as intrauterine devices , contraceptives or condoms) ；No pregnant or breastfeeding women, and a negative pregnancy test are received within 7 days before the randomization.

Exclusion Criteria:

  1. Has other non-epithelial ovarian tumors or borderline ovarian epithelial tumors;

  2. Other malignant tumors that have appeared or are currently present within 5 years, except for cured cervical carcinoma in situ, non-melanoma skin cancer and superficial bladder tumors;

  3. Has previously received immune drugs such as PD-1 / PD-L1, CTLA-4 or other tyrosine kinase inhibitors such as anlotinib hydrochloride;

  4. Has received bevacizumab within 28 days before the first dose;

  5. Has received chemotherapy, surgery, radiotherapy, the last treatment from the first dose less than 4 weeks, or oral targeted drugs for less than 5 half-lives, or oral fluorouracil pyridine drugs for less than 14 days, mitomycin C and nitrosourea for less than 6 weeks;

  6. Expect to use any active vaccine against infectious diseases (such as influenza vaccine, chickenpox vaccine, etc.) within 28 days before the first dose or during the study period;

  7. Patients diagnosed with immunodeficiency or undergoing systemic glucocorticoid therapy or any other form of immunosuppressive therapy (dose> 10mg / day prednisone or other effective hormones) and continue to use it within 2 weeks before the first dose;

  8. Active autoimmune diseases that require systemic treatment have occurred within 2 years before the first dose;

  9. Subjects known to be allergic to the study drug or any of its excipients or have experienced a severe allergic reaction to other monoclonal antibodies;

  10. Has uncontrollable symptoms of brain metastases, spinal cord compression, cancerous meningitis;

  11. Has any bleeding or bleeding event ≥ CTC AE Grade 3 or unhealed wounds, ulcers or fractures within 4 weeks before the first dose;

  12. Has clinically significant thyroid dysfunction before the first dose;

  13. Has multiple factors affecting oral medication;

  14. Has any severe acute complications before the first dose;

  15. Has participated in other anti-tumor intervention clinical trials within 4 weeks before the first medication;

  16. According to the judgement of the researchers, there are other factors that may lead to the termination of the study. For example, other serious diseases including mental disorders need to be treated together, serious laboratory abnormalities, accompanied by family or social factors, which will affect the safety of the subjects, or the collection of data and samples.

Contacts and Locations

Locations

Site City State Country Postal Code
1 The General Hospital of the People's Liberation Army Beijing Beijing China 100039
2 Cancer Hospital of Chongqing University Chongqing Chongqing China 400030
3 The First Hospital of Lanzhou University Lanzhou Gansu China 730000
4 Sun Yat-sen University Cancer Center Guangzhou Guangdong China 510000
5 First Hospital of Qinhuangdao Qinhuangdao Hebei China 066000

Sponsors and Collaborators

  • Chia Tai Tianqing Pharmaceutical Group Co., Ltd.

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Chia Tai Tianqing Pharmaceutical Group Co., Ltd.
ClinicalTrials.gov Identifier:
NCT04236362
Other Study ID Numbers:
  • TQB2450-Ib-10
First Posted:
Jan 22, 2020
Last Update Posted:
Jan 12, 2021
Last Verified:
Jan 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Jan 12, 2021