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NCT05735327Active, not recruiting

A Study of Brigatinib as Preferred First Therapy for Adults With Non-Small Cell Lung Cancer (NSCLC) ENTIRETY

Effectiveness and Safety of Brigatinib Treatment as First-line Therapy Administered to ALK Positive Non-Small Cell Lung Cancer (NSCLC) Patients. Prospective, Multicenter, Observational Study

Source: ClinicalTrials.gov · Last updated 13 Apr 2026

Brief summary (registry, in English)

This is a study of brigatinib in adults with Non-Small Cell Lung Cancer (NSCLC). The main aim of this study is to learn about the time period in which the condition does not worsen after the participant has received brigatinib. Another aim is to learn about the overall rate of participants who respond to the treatment with brigatinib. Participants will receive brigatinib as part of their normal clinical practice. Data will be collected during regular visits to the hospital (a total of up to 12 visits is planned throughout study duration).

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
50 (estimated)
First submitted
10 Feb 2023
Start date
22 May 2023
Primary completion date
26 Apr 2027
Lead sponsor
Takeda
Diseases
Lung cancer
NCT number
NCT05735327

What you commit to

  • Study type: Observational
  • Planned participants: 50
  • From 22 May 2023 to the primary completion date, 26 Apr 2027
  • 12 sites in 1 country
  • 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

  • Current or planned participation in an interventional clinical trial for ALK positive non-small cell lung cancer (NSCLC).

Other

  • Cognitive incapacity, unwillingness or language barriers precluding adequate understanding or cooperation.

Who the study is looking for

  • Adult (aged ≥18) ALK positive NSCLC participants receiving brigatinib as a first-line treatment in the scope of NDP.
  • Participants willing to participate in the study and signed ICF.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (12)

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

SiteCityCountrySite status
Centrum Onkologii im. Prof. F. Lukaszczyka w Bydgoszczy
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BydgoszczPolandUnknown status
Centrum Pulmonologii i Torakochirurgii w Bystrej
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BystraPolandUnknown status
Krakowski Szpital Specjalistyczny im. Jana Pawla II w Krakowie
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KrakowPolandUnknown status
Narodowy Instytut Onkologii im. Marii Sklodowskiej-Curie- Panstwowy Instytut Badawczy Oddzial w Krakowie
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KrakowPolandUnknown status
SPZOZ Uniwersytecki Szpital Kliniczny nr 2 im. Wojskowej Akademii Medycznej Uniwersytetu Medycznego w Lodzi Centralny Szpital Weteranow
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LodzPolandUnknown status
Samodzielny Publiczny Szpital Kliniczny Nr 4 w Lublinie
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LublinPolandUnknown status
Wielkopolskie Centrum Pulmonologii i Torakochirurgii w Poznaniu
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PoznanPolandUnknown status
Szpital Kliniczny im. Heliodora Swiecickiego UM wPoznaniu.
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PoznanPolandUnknown status
Podkarpackie Centrum Chorob Pluc
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RzeszówPolandUnknown status
Narodowy Instytut Onkologii im Marii Sklodowskiej Curie Panstwowy Instytut Badawczy
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WarsawPolandUnknown status
Instytut Gruzlicy I Chorob Pluc
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WarsawPolandUnknown status
Dolnoslskie Centrum Onkologii, Pulmonologii i Hematologii
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WroclawPolandUnknown status

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