Phase 2 Lymphoma Trial, Recruiting NCT07418190 Sponsor: The First Affiliated Hospital with Nanjing Medical University Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT07418190
Recruiting Phase 2

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 18 years of age or older
  • People who have been diagnosed with follicular lymphoma (a type of slow-growing blood cancer) that has come back or stopped responding to treatment, confirmed by a tissue sample test
  • People who have already received at least two previous rounds of cancer treatment, including at least one treatment that targeted a protein called CD20 on cancer cells
  • People who are generally well enough to carry out daily activities (the trial uses a standard medical scale to measure this, rated 0 or 1 out of 4)
  • People who have at least one measurable area of disease larger than 1.5 cm
  • People whose life expectancy is estimated by their doctor to be at least 18 weeks
  • People whose side effects from previous cancer treatments have mostly cleared up (to a mild level or below), apart from hair loss or reduced appetite
  • People whose liver is functioning adequately, based on blood test results within accepted ranges
  • People whose blood counts (white blood cells, platelets, and red blood cells) are within acceptable levels, without having needed a blood or platelet transfusion very recently
  • People whose kidneys are functioning adequately, based on blood test results
  • Women who could become pregnant must have a negative pregnancy test within 7 days before starting treatment, and must agree to avoid pregnancy during the study through abstinence or effective contraception
  • Men must agree to avoid fathering a child during the study through abstinence or effective contraception

Who may not be able to join:

  • People who are unable to follow the requirements of the trial, including any required hospital stays or restrictions
  • People who have an active infection or a latent (inactive but present) tuberculosis infection
  • People who have had a serious allergic reaction to medicines in the same drug class as the trial treatment
  • People whose lymphoma has spread to the brain or spinal cord
  • People who are pregnant or breastfeeding
  • People with serious uncontrolled health conditions, such as heart disease or immune system disorders, or who have had a heart attack, dangerous irregular heartbeat, or unstable chest pain within the past 6 months
  • People with a history of illicit drug use or alcohol misuse within the 12 months before screening, based on the doctor's assessment
  • People with any other medical condition, abnormal test result, or health finding that the trial doctor believes makes the trial treatment unsuitable for them
  • People with a psychiatric condition or memory/thinking difficulties that may prevent them from understanding or following the trial requirements
  • People (or their partners) planning to become pregnant during the study period
  • People whom the trial doctor considers unsuitable for participation for any other reason

People already enrolled may be excluded from the trial's results analysis if:

  • It is discovered after joining that they did not meet the eligibility criteria
  • They had previously been treated with zanubrutinib or similar drugs called BTK inhibitors
  • They experienced intolerable side effects from zanubrutinib or similar drugs
  • They received fewer than two doses of the trial treatment, making it impossible to assess whether it worked
  • There were violations of the trial rules
  • They had previously undergone a stem cell transplant using donor or their own stem cells

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 13 July 2026
Phase 2: approximately ~30% 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

Principal Investigator: Wei Xu, PhD, Hematological Department, Jiangsu Province Hospital

Phone: 15952032421

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 2
Registry
ClinicalTrials.gov
Start date
1 February 2026
Est. completion
31 December 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Complete response rate (CRR)

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: 13 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