Phase 1 Lymphoma Trial, Recruiting NCT04651348 Sponsor: Beijing Mabworks Biotech Co., Ltd. Condition: Lymphoma
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Phase 1 Lymphoma Trial, Recruiting

NCT04651348
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 or older
  • People who have been diagnosed with a lymphoma or solid tumour that has come back or has not responded to previous treatment
  • People whose general physical health and ability to carry out daily activities is rated as fully active or restricted in strenuous activity only (this is measured using a standard scale called ECOG; confirm with trial site)
  • People with a life expectancy of at least 3 months
  • People whose organs (such as kidneys and liver) and bone marrow are functioning well enough to meet the trial's requirements (confirm with trial site)
  • People who have at least one tumour that can be measured or assessed using standard imaging methods
  • People who are willing and able to give written consent and follow the study requirements

Who may not be able to join:

  • People who have received any anti-cancer treatment (such as chemotherapy, radiation, targeted therapy, or immunotherapy) within 4 weeks before the trial starts
  • People who have previously been treated with a drug that targets proteins called CD47 or SIRPα
  • People who have had major surgery within 4 weeks before the trial starts, or who are expected to have major surgery during the trial
  • People who have received a live vaccine within 4 weeks before the trial starts, or who would need one during the trial
  • People who have cancer that has spread to the brain or spinal cord
  • People who have had a different type of cancer within the past 5 years
  • People who have another serious, uncontrolled medical condition
  • People who have HIV, hepatitis B, or hepatitis C infection (specific blood test results apply; confirm with trial site)
  • People who have an active or suspected autoimmune disease
  • Women who could become pregnant, unless they agree to use two reliable forms of contraception, or to avoid heterosexual intercourse, both during the trial and for at least 12 months after all treatment ends
  • People with a known history of a condition where the body destroys its own red blood cells (haemolytic anaemia)
  • People who have had a known severe allergic reaction or serious reaction to a monoclonal antibody treatment in the past

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 21 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: (+86)010-88121122

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
Beijing Mabworks Biotech Co., Ltd.
Registry
ClinicalTrials.gov
Start date
4 January 2021
Est. completion
8 December 2022

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Percentage of Participants with Adverse Events

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: 21 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