Skip to main content
OpenTrials
Recruiting

NCT Number: NCT05532696

Phase 1b/2 Study to Evaluate ABT-101 in Solid Tumor and NSCLC Patients

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)

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

Taichung Veterans General Hospital, Taichung, Taiwan

Loading trial locations.

About this study

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

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or female aged ≥ 20 years or adult age as per local regulations, at time of informed consent
  • Histologically or cytologically confirmed advanced solid tumor (Part 1) or NSCLC with HER2 mutations as determined by the central result (Part 2)
  • For patients in Part 2 only: Patients has measurable disease per RECIST 1.1 criteria
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 (Part 1), 0 to 2 (Part 2)
  • Appropriate candidate for experimental therapy
  • Adequate organ function

Exclusion criteria

  • Known active or untreated central nervous system (CNS) metastases and/or carcinomatous meningitis
  • For patients in Part 2 only: Previously treated with EGFR or HER2 TKIs.
  • Serious acute or chronic infections
  • Received a live-virus vaccination
  • Received prior anticancer or other investigational therapy within 28 days or 5× the half-life prior to the first dose.
  • Not recovered from prior- treatment toxicities to Grade ≤1
  • Major surgery within 28 days prior to the study treatment
  • Concurrent malignancy within 2 years prior to first dose
  • History or presence of clinically relevant cardiovascular abnormalities. QTcF ≥ 470 ms
  • Significant gastrointestinal disorder(s) that could interfere with absorption of ABT101
  • Known to have a history of alcoholism or drug abuse

Treatment and study plan

ABT-101

Drug

Patients will receive ABT-101 by oral administration on a 28-day cycle

Other names: DBPR112

Primary outcomes

  1. Determine the recommended Phase 2 Dose (RP2D) of ABT-101 in Part 1

    Time frame: 18 months

    Determine the maximum tolerated dose (MTD) and RP2D of ABT-101 based on Dose Limiting Toxicities

  2. Determine antitumor activity based on Objective Response Rate (ORR) in Part 2 in patients with NSCLC with targeted mutation

    Time frame: 36 months

    Patients response according to RECIST 1.1

Secondary outcomes

  1. Maximum plasma concentration (Cmax) ABT-101

    Time frame: 48 months

    Plasma concentration of ABT-101

  2. Area under the plasma concentration time curve (AUC) of ABT-101

    Time frame: 48 months

    Measure of AUC

  3. Duration of response (DOR)

    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

  4. Progression- free survival (PFS)

    Time frame: 36 months

    Measure of the time from study entry to disease progression or death due to any cause

  5. Overall survival (OS)

    Time frame: 36 months

    Measure of overall survival

  6. Objective response rate (ORR) in Part 1

    Time frame: 12 months

    Objective response rate as determined by RECIST 1.1

  7. Disease control rate (DCR)

    Time frame: 36 months

    DCR is defined as the percentage of patients who have achieved a CR, PR, or SD.

Study contacts

Contact information is provided by the study sponsor or research team.

Sponsors and collaborators

Lead sponsor

Anbogen Therapeutics, Inc.

Industry

Registry information

Official study title

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

Important dates

Study start
2022
Primary completion
2026
Study completion
2027
First posted
Sep 8, 2022
Registry last updated
Jun 24, 2024

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.

Published trials that share one or more normalized conditions with this study.