Phase 2 Lung Cancer Trial, Recruiting NCT05532696 Sponsor: Anbogen Therapeutics, Inc. Condition: Lung Cancer
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Phase 2 Lung Cancer Trial, Recruiting

NCT05532696
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People aged 20 years or older (or adult age as defined by local rules) at the time of signing consent
  • People who have an advanced solid tumour confirmed by laboratory testing of tissue or cells (Part 1 of the trial), or people who have non-small cell lung cancer (NSCLC) with a specific HER2 gene mutation confirmed by a central laboratory test (Part 2 of the trial)
  • People in Part 2 only: those whose cancer can be measured using standard imaging criteria (called RECIST 1.1)
  • People whose general health and ability to carry out daily activities meets a specific score — either a score of 0 or 1 for Part 1, or 0 to 2 for Part 2 (confirm with trial site what these scores mean for eligibility)
  • People whose heart, liver, kidneys, and other organs are functioning well enough to meet the trial's requirements
  • People considered a suitable candidate for experimental treatment by their treating doctor

Who may not be able to join:

  • People with known active or untreated cancer that has spread to the brain or the lining around the brain or spinal cord
  • People in Part 2 only: those who have previously been treated with certain targeted therapies that act on the EGFR or HER2 proteins (called TKIs)
  • People with a serious active or ongoing infection
  • People who have recently received a live-virus vaccine
  • People who have received cancer treatment or other experimental therapy within the past 28 days, or within a timeframe based on how long the previous treatment stays active in the body
  • People who have not yet recovered from side effects of previous cancer treatment (side effects must have reduced to a mild level or resolved)
  • People who have had major surgery within 28 days before starting the trial
  • People who have had another separate cancer diagnosis within the past 2 years
  • People with a significant or clinically relevant heart condition, or whose heart electrical reading (called QTcF interval) is 470 milliseconds or longer
  • People with significant digestive system problems that could affect how the trial drug (ABT101) is absorbed by the body
  • People with a known history of alcohol or drug abuse

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Phone: +886-2-2742-1839

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Anbogen Therapeutics, Inc.
Registry
ClinicalTrials.gov
Start date
27 September 2022
Est. completion
1 November 2026

Where this trial is recruiting

🇹🇼 Taiwan

Primary endpoints

Determine the recommended Phase 2 Dose (RP2D) of ABT-101 in Part 1; Determine antitumor activity based on Objective Response Rate (ORR) in Part 2 in patients with NSCLC with targeted mutation

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov