← Back to Clinical Trials
Recruiting Phase 2 NCT06664411

NCT06664411 Pola-ZR2P in Previously Untreated DLBCL

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT06664411
Status Recruiting
Phase Phase 2
Sponsor Navy General Hospital, Beijing
Condition Diffuse Large B-cell Lymphoma
Study Type INTERVENTIONAL
Enrollment 80 participants
Start Date 2024-09-24
Primary Completion 2029-12

Eligibility & Interventions

Sex All sexes
Min Age 14 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Polatuzumab Vedotin, Zanubrutinib, Rituximab, Lenalidomide and Prednisone as Induction Therapy

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

In Phase 2, researchers evaluate early signs of effectiveness. You may be randomized to receive the active treatment or a comparator. Monitoring continues closely.

This trial targets 80 participants in total. It began in 2024-09-24 with a primary completion date of 2029-12.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The goal of this phase 2 trial is to test the safety and efficacy of Pola-ZR2P as induction therapy in patients with DLBCL.

Eligibility Criteria

Inclusion Criteria: * Pathologically confirmed Diffuse Large B Cell Lymphoma according World Health Organization (WHO) classification; * Patient is ≥ 18 years of age at the time of signing the informed consent form (ICF). * Patient must understand and voluntarily sign an ICF prior to any study-specific assessments/procedures being conducted; * Patient is willing and able to adhere to the study visit schedule and other protocol requirements; * Patient has not received chemotherapy previously. * Anticipated life expectancy at least 3 months Exclusion Criteria: * Active or uncontrolled infections requiring systemic treatment within 14 days before enrollment. * Any instability of systemic disease, including but not limited to severe cardiac, liver, kidney, or metabolic disease need therapy. * Pregnant or lactating women

Contact & Investigator

Central Contact

Liren Qian, PhD

✉ qlr2007@126.com

📞 +861066947194

Principal Investigator

Liren Qian, PhD

PRINCIPAL INVESTIGATOR

Navy General Hospital, Beijing

Frequently Asked Questions

Who can join the NCT06664411 clinical trial?

This trial is open to participants of all sexes, aged 14 Years or older, studying Diffuse Large B-cell Lymphoma. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

What phase is the NCT06664411 trial and what does that mean for participants?

Phase 2 trials evaluate whether the treatment shows signs of effectiveness while continuing to monitor safety. More participants are enrolled than in Phase 1 to help refine the treatment protocol.

Is NCT06664411 currently recruiting?

Yes, NCT06664411 is actively recruiting participants. Contact the research team at qlr2007@126.com for enrollment information.

Where is the NCT06664411 trial being conducted?

This trial is being conducted at Beijing, China.

Who is sponsoring the NCT06664411 clinical trial?

NCT06664411 is sponsored by Navy General Hospital, Beijing. The principal investigator is Liren Qian, PhD at Navy General Hospital, Beijing. The trial plans to enroll 80 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology