Phase 1 Lymphoma 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:
- People who are able to understand and are willing to sign a consent form
- People aged 18 or older
- People who have a confirmed advanced solid tumour that has stopped responding to standard treatments, has no standard treatment available, or who have a type of blood cancer called non-Hodgkin lymphoma that has come back or stopped responding after at least 2 previous treatments
- People with an advanced solid tumour who have at least one tumour that can be measured using standard imaging criteria
- People with non-Hodgkin lymphoma whose cancer can be measured or assessed using standard lymphoma response criteria
- People with a general health/activity level rating of 0, 1, or 2 on a standard medical scale (meaning able to carry out most daily activities, with or without some limitations) (confirm with trial site)
- People who are able to provide a tissue sample from their tumour
- People with a life expectancy of at least 12 weeks
Who may not be able to join:
- People with a known history of severe allergic reaction to any ingredient in the trial drug HCB101
- People with active or untreated cancer that has spread to the brain or the lining around the brain
- People who have had major surgery, intensive radiotherapy, palliative radiotherapy, or a radioactive drug treatment that was not completed at least 2 weeks before the trial would start
- People with a significant heart or blood vessel condition
- People still experiencing side effects from previous cancer treatments that have not returned to a mild or baseline level (with the exception of hair loss and anaemia)
- People with a known inherited or acquired bleeding disorder
- People who have had a red blood cell transfusion within 4 weeks before screening
- People who have been diagnosed with a condition causing the body to destroy its own red blood cells (haemolytic anaemia or Evans Syndrome) in the past 3 months
- People currently receiving any other systemic cancer treatment, whether experimental or approved
- People currently taking a blood-thinning medication called a vitamin K antagonist (such as warfarin); certain other blood thinners may be considered on a case-by-case basis (confirm with trial site)
- People who have used herbal medicines within 14 days before the trial would start
- People who have previously received any treatment that targets the CD47 or SIRPα pathway (confirm with trial site)
- People who have had another cancer requiring treatment within the past 2 years
- People who have participated in another clinical trial using an experimental treatment within the past 14 days
- People who have used an experimental medical device within the past 28 days
- People who test positive for hepatitis B, active hepatitis C, HIV, or have known active or latent tuberculosis
- People with a known history of alcohol or drug misuse
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: +886-2-27921366
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
Number/incidence and percentage of subjects with adverse events, including ADA.; Number of subjects with MTD of HCB101
Can't join this trial?
Data last synced from ClinicalTrials.gov: 20 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.