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A Study of TQ-B3101 Capsules in Subjects With Advanced Malignant Tumor

C

CTTQ

Status and phase

Unknown
Phase 2

Conditions

Advanced Malignant Tumor

Treatments

Drug: TQ-B3101

Study type

Interventional

Funder types

Industry

Identifiers

NCT04412564
TQ-B3101-II-03

Details and patient eligibility

About

The objective of this study is to evaluate efficacy and safety of TQ-B3101 in subjects with advanced malignant tumor.

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

-1. Eastern Cooperative Oncology Group (ECOG) performance status score of 0 to 1; Life expectancy ≥12 weeks.

  1. Understood and signed an informed consent form. 3. Histologically or cytologically confirmed advanced malignant solid tumors. 4. Adequate organ system function. 5. Patients need to adopt effective methods of contraception.

Exclusion criteria

    1. Has multiple factors affecting oral medication. 2. The toxicity of previous antitumor treatment is not recovered to ≤ grade 1. 3. Other malignancies occurred within 3 years, with exception of cured cervical carcinoma in situ, non-melanoma skin cancer and superficial bladder tumors.

    2. Has a history of hypertension, hypertensive encephalopathy or uncontrolled hypertension.

    3. Has cardiovascular and cerebrovascular diseases. 6. Has received radiotherapy, chemotherapy, surgery less than 4 weeks before the first dose.

    4. Has central nervous system metastasis and / or spinal cord compression, cancerous meningitis, and meningeal disease.

    5. Active hepatitis, HIV positive, syphilis positive. 9. Has a history of psychotropic substance abuse. 10. According to the judgement of the researchers, there are other factors that subjects are not suitable for the study.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

200 participants in 1 patient group

TQ-B3101 capsules
Experimental group
Description:
TQ-B3101 capsules 300mg bid administered orally in 28-day cycle.
Treatment:
Drug: TQ-B3101

Trial contacts and locations

36

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Central trial contact

Hongming Pan, Doctor

Data sourced from clinicaltrials.gov

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