ABT-101
DrugPatients will receive ABT-101 by oral administration on a 28-day cycle
Other names: DBPR112
NCT Number: NCT05532696
A Phase 1b/2, open-label, multicenter study to determine the recommended phase 2 (RP2D) of ABT-101in solid tumor and to explore antitumor activities of ABT-101 in patients with HER 2 mutated non-small cell lung cancer (NSCLC)
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 1 / Phase 2
Taichung Veterans General Hospital, Taichung, Taiwan
This study will be conducted in two parts:
Part 1: Dose- Escalation, Phase 1b, is designed to determine the RP2D. Patients with solid tumor will be enrolled into a dose finding study scheme with the assessment of dose-limiting toxicities (DLTs). DLT assessment will be conducted during treatment cycle 1
Part 2: Dose- Expansion, Phase 2, will evaluate the safety and efficacy of ABT-101 at the dosage and dosing regime determined in Phase 1b. Phase 2 will enroll NSCLC patients with HER2 mutations
Study participation for all patients includes screening period, treatment period and safety/ follow-up period. Patient will received study treatment until progressive disease or any other discontinuation or withdrawal criterion is met
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients will receive ABT-101 by oral administration on a 28-day cycle
Other names: DBPR112
Time frame: 18 months
Determine the maximum tolerated dose (MTD) and RP2D of ABT-101 based on Dose Limiting Toxicities
Time frame: 36 months
Patients response according to RECIST 1.1
Time frame: 48 months
Plasma concentration of ABT-101
Time frame: 48 months
Measure of AUC
Time frame: 48 months
DOR is defined as the length of time between first response and the date of objectively documented progression of disease or death
Time frame: 36 months
Measure of the time from study entry to disease progression or death due to any cause
Time frame: 36 months
Measure of overall survival
Time frame: 12 months
Objective response rate as determined by RECIST 1.1
Time frame: 36 months
DCR is defined as the percentage of patients who have achieved a CR, PR, or SD.
Contact information is provided by the study sponsor or research team.
Anbogen Therapeutics, Inc.
Industry
A Phase Ib/II, Open-Label, Multicenter Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Antitumor Activity of ABT-101 in Patients With Advanced Solid Tumors and HER2 Exon 20 Insertions Mutated Non- Small Cell Lung Cancer
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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