Phase 1 Lung Cancer Trial, Recruiting NCT06621563 Sponsor: Hansoh BioMedical R&D Company Condition: Lung Cancer
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Phase 1 Lung Cancer Trial, Recruiting

NCT06621563
Recruiting Phase 1

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:

  • Adults aged 18 to 75 years old (inclusive)
  • People with a cancer diagnosis that has been confirmed by laboratory tissue testing, where the cancer cannot be surgically removed, has come back, or has spread to other parts of the body
  • People who have at least one measurable tumour that can be tracked during the trial (as assessed using standard imaging guidelines called RECIST v1.1)
  • People who are generally well enough to carry out everyday activities with little or no limitation (assessed using a standard scale called ECOG, scored 0 or 1)
  • People with a life expectancy of more than 12 weeks
  • People who are willing and able to use adequate contraception throughout the study
  • Women who are not pregnant at the start of the trial, or who are confirmed to be unable to become pregnant
  • People who have read, understood, and signed the trial's consent form

Who may not be able to join:

  • People who have previously received, or are currently receiving, any cancer treatment that targets a protein called MET, including targeted therapy pills (TKIs), antibodies, or antibody-drug conjugates
  • People who have previously received, or are currently receiving, antibody treatments that target a protein called EGFR
  • People who have received systemic anti-cancer treatment (including chemotherapy, certain traditional Chinese medicine anti-cancer treatments, or targeted therapy pills) within 2 weeks before the first dose of the trial drug
  • People who have received any other experimental anti-cancer drugs, antibodies, or antibody-drug conjugates within 4 weeks before the first dose of the trial drug
  • People who have had localised radiotherapy within 2 weeks before the first dose, or large-area radiotherapy (including treatment covering more than 30% of the bone marrow) within 4 weeks before the first dose
  • People who have fluid build-up around the lungs or in the abdomen that requires medical treatment, or fluid around the heart
  • People who have had major surgery within 4 weeks before the first dose of the trial drug
  • People who still have significant side effects (Grade 2 or higher) from previous cancer treatments
  • People who have a second active cancer that has not been fully treated
  • People who have cancer that has spread to the brain or spinal cord and has not been treated, or is currently active
  • People with severe, uncontrolled, or active heart or blood vessel conditions
  • People who have had a serious infection within 4 weeks before the first dose of the trial drug

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 16 July 2026
Phase 1: approximately ~10% 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: 13061877102

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 1
Sponsor
Hansoh BioMedical R&D Company
Registry
ClinicalTrials.gov
Start date
14 December 2024
Est. completion
30 March 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Incidence and severity of treatment-emergent adverse events; Tolerability of HS-20117 combination therapy: incidence of DLT events, maximum tolerated dose (MTD) or maximum applicable dose (MAD) of HS-20117 in combination therapies.

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: 16 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