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NCT05160922Active, not recruitingPhase 4

Crizotinib Continuation Clinical Study

CRIZOTINIB MASTER PROTOCOL: AN OPEN-LABEL CONTINUATION STUDY FOR PARTICIPANTS CONTINUING FROM PFIZER-SPONSORED CRIZOTINIB CLINICAL STUDIES

Source: ClinicalTrials.gov · Last updated 30 Mar 2026

Brief summary (registry, in English)

The purpose of this continuation study is to provide continued access to crizotinib treatment for eligible participants from a current Pfizer sponsored crizotinib clinical study that is planned to close.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
27 (actual)
First submitted
6 Dec 2021
Start date
27 Dec 2021
Primary completion date
21 Mar 2028
Lead sponsor
Pfizer
NCT number
NCT05160922
EU CT number
2024-511128-15-00

What you commit to

  • Study type: Interventional · Phase 4
  • Participants enrolled: 27
  • From 27 Dec 2021 to the primary completion date, 21 Mar 2028
  • 13 sites in 5 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Participants with any of the following characteristics/conditions will be excluded:

Other

  • Female participants who are pregnant or breastfeeding.
  • Any medical reason that, in the opinion of the investigator or sponsor, precludes the participant from inclusion in the study.

Criteria the registry did not label

  • Participants must meet the following key inclusion criteria to be eligible for enrollment into the study:
  • Any participant who is receiving crizotinib and deriving clinical benefit (as determined by their doctor) in a Crizotinib Study which is planned to close.
  • Participants must agree to follow the reproductive criteria as outlined in protocol.
  • No ongoing Grade ≥3 or intolerable Grade 2 AEs considered to be related to crizotinib treatment, except for those laboratory eligibility criteria described in Inclusion #4.
  • Adult Participants (≥18 years): Adequate hepatic and bone marrow function. Stable renal function for at least 14 days.
    • Pediatric Participants (\<18 years): Adequate hepatic and bone marrow function. Stable renal function for at least 14 days.

Age in the registry: 0 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (13)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Cancer Hospital Chinese Academy of Medical Science
Coordinator of this site? Confirm its status
BeijingChinaUnknown status
Beijing Cancer Hospital
Coordinator of this site? Confirm its status
BeijingChinaUnknown status
Jilin Cancer Hospital
Coordinator of this site? Confirm its status
ChangchunChinaUnknown status
Fujian Province Oncology Hospital
Coordinator of this site? Confirm its status
FuzhouChinaUnknown status
The First Affiliated Hospital of Guangzhou Medical University
Coordinator of this site? Confirm its status
GuangzhouChinaUnknown status
Sun Yat-sen University Cancer Center
Coordinator of this site? Confirm its status
GuangzhouChinaUnknown status
The First Affiliated Hospital of College of Medicine,Zhejiang University
Coordinator of this site? Confirm its status
HangzhouChinaUnknown status
Shanghai Chest Hospital
Coordinator of this site? Confirm its status
ShanghaiChinaUnknown status
West China Hospital of Sichuan University
Coordinator of this site? Confirm its status
Wuhou DistrictChinaUnknown status
ASST Monza
Coordinator of this site? Confirm its status
MonzaItalyUnknown status
National Hospital Organization Nagoya Medical Center
Coordinator of this site? Confirm its status
NagoyaJapanUnknown status
Limited Liability Company "EuroCityClinic"
Coordinator of this site? Confirm its status
Saint PetersburgRussiaUnknown status
National Taiwan University Hospital
Coordinator of this site? Confirm its status
TaipeiTaiwanUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.