Patient Guide: A Safety and Preliminary Efficacy Study of CC-99282, Alone and in Combination With Anti-lymphoma Agents in Participants With Relapsed or Refractory Non-Hodgkin Lymphomas (R/R NHL)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 66 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT03930953
Status: ACTIVE_NOT_RECRUITING
Condition: Lymphoma, Non-Hodgkin
Phase: PHASE1, PHASE2

Where You Can Participate

This study is available at 66 locations across the country.

Top locations include:
  • • Scottsdale, Arizona
  • • Jacksonville, Florida
  • • Tampa, Florida
  • • And 63 more locations

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A Safety and Preliminary Efficacy Study of CC-99282, Alone and in Combination With Anti-lymphoma Agents in Participants With Relapsed or Refractory Non-Hodgkin Lymphomas (R/R NHL) - Join Clinical Trial NCTNCT03930953

How to Join This Clinical Trial - NCTNCT03930953

Learn how to participate in this PHASE1, PHASE2 trial studying an investigational therapy for Lymphoma, Non-Hodgkin. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Lymphoma, Non-Hodgkin. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Lymphoma, Non-Hodgkin
Treatment Being Tested
Investigational treatment
Study Phase
PHASE1, PHASE2 - Safety and effectiveness study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT03930953 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 66 locations. Find a study site near you:

Clinical Research Site

Scottsdale, Arizona 85259 - United States

Status: Contact for availability

Clinical Research Site

Jacksonville, Florida 32224 - United States

Status: Contact for availability

Clinical Research Site

Tampa, Florida 32207 - United States

Status: Contact for availability

Clinical Research Site

Overland Park, Kansas 66210 - United States

Status: Contact for availability

Clinical Research Site

Rochester, Minnesota 55905 - United States

Status: Contact for availability

Clinical Research Site

Saint Louis, Missouri 63110 - United States

Status: Contact for availability

Clinical Research Site

Hackensack, New Jersey 07601 - United States

Status: Contact for availability

Clinical Research Site

Houston, Texas 77030 - United States

Status: Contact for availability

Clinical Research Site

Ciudad Autonoma de Buenos Aires, Buenos Aires C1118AAT - Argentina

Status: Contact for availability

Clinical Research Site

Pilar, Buenos Aires 1629 - Argentina

Status: Contact for availability

And 56 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE1, PHASE2 clinical trial for Lymphoma, Non-Hodgkin:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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