Phase 1 Lung Cancer Trial, Recruiting
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.
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
Where this trial is recruiting
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?
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.