Phase 1 Lymphoma Trial, Recruiting NCT05892718 Sponsor: FBD Biologics Limited Condition: Lymphoma
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Phase 1 Lymphoma Trial, Recruiting

NCT05892718
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:

  • 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.

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 20 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: +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

Status
Recruiting
Phase
Phase 1
Sponsor
FBD Biologics Limited
Registry
ClinicalTrials.gov
Start date
2 October 2023
Est. completion
30 May 2027

Where this trial is recruiting

🇨🇳 China 🇹🇼 Taiwan 🇺🇸 United States

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?

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: 20 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