Patient Guide: Study of the Effect of Rifampicin on the Pharmacokinetics (PK) of Multiple Doses of Cediranib in Patients With Solid Tumours

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 6 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT00750841
Status: ACTIVE_NOT_RECRUITING
Condition: Solid Tumors
Phase: PHASE1

Where You Can Participate

This study is available at 6 locations across the country.

Top locations include:
  • • Edmonton, Alberta
  • • Montreal, Quebec
  • • Dundee,
  • • And 3 more locations

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Study of the Effect of Rifampicin on the Pharmacokinetics (PK) of Multiple Doses of Cediranib in Patients With Solid Tumours - Join Clinical Trial NCTNCT00750841

How to Join This Clinical Trial - NCTNCT00750841

Learn how to participate in this PHASE1 trial studying an investigational therapy for Solid Tumors. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Solid Tumors
Treatment Being Tested
Investigational treatment
Study Phase
PHASE1 - Early safety study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT00750841 - 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 6 locations. Find a study site near you:

Clinical Research Site

Edmonton, Alberta T6G 1Z2 - Canada

Status: Contact for availability

Clinical Research Site

Montreal, Quebec H3T 1E2 - Canada

Status: Contact for availability

Clinical Research Site

Dundee, DD1 9SY - United Kingdom

Status: Contact for availability

Clinical Research Site

Glasgow, G12 0YN - United Kingdom

Status: Contact for availability

Clinical Research Site

London, NW1 2PG - United Kingdom

Status: Contact for availability

Clinical Research Site

London, SE1 9RT - United Kingdom

Status: Contact for availability

How to Enroll in This Study

To learn more about participating in this PHASE1 clinical trial for Solid Tumors:

  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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