Clinical Trials Directory

Trials / Unknown

UnknownNCT04273815

A Study to Evaluate the Tolerance, Pharmacokinetics and Efficacy of TQ-A3334 Tablets

A Phase Ib, Open-label, Dose Escalation and Expansion Study to Evaluate the Tolerance , Pharmacokinetics and Effectiveness of TQ-A3334 Tablets in Patients With Advanced Non-small Cell Lung Cancer

Status
Unknown
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
40 (estimated)
Sponsor
Chia Tai Tianqing Pharmaceutical Group Co., Ltd. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This is a study to evaluate the tolerance, dose-limiting toxicity (DLT), and maximum tolerated dose (MTD) of single and multiple oral doses of TQ-A3334 and observe the efficacy of TQ-A3334 in combination with anlotinib capsules in patients with non-small cell lung cancer.

Conditions

Interventions

TypeNameDescription
DRUGTQ-A3334TQ-A3334 is a highly efficient and highly selective TLR-7 agonist. TLR-7 can induce the release of a series of pro-inflammatory cytokines, including IFN-α (interferon-α), IL-12 (Interleukin 12), TNF-α, and promote the maturation and antigen presentation of dendritic cells, play an antitumor effect.
DRUGAnlotinibAnlotinib is a multi-target receptor tyrosine kinase inhibitor.

Timeline

Start date
2020-07-06
Primary completion
2021-01-31
Completion
2021-01-31
First posted
2020-02-18
Last updated
2020-07-08

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT04273815. Inclusion in this directory is not an endorsement.