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Real-World Observational Study of Iruplinalkib in the Treatment of ALK-Positive Non-Small Cell Lung Cancer

Real-World Observational Study of Iruplinalkib in the Treatment of ALK-Positive Non-Small Cell Lung Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500114592
Enrollment
Unknown
Registered
2025-12-15
Start date
2025-12-15
Completion date
Unknown
Last updated
2026-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Locally Advanced or Metastatic Anaplastic Lymphoma Kinase (ALK)-Positive Non-Small Cell Lung Cancer (NSCLC)

Interventions

Observation Group for ALK-positive non-small cell lung cancer treatment:None

Sponsors

Shandong First Medical University and Shandong Academy of Medical Sciences (Shandong Cancer Hospital &Institute)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Patients voluntarily sign the informed consent form (ICF); 2.Age = 18 years old, regardless of gender; 3.Patients with pathologically confirmed locally advanced or metastatic ALK-positive non-small cell lung cancer (NSCLC); 4.Planned to receive iruplinalkib treatment.

Exclusion criteria

Exclusion criteria: Patients who meet any of the following conditions will be prohibited from enrolling in this study: 1. Mental abnormalities or inability to cooperate with examinations or follow-ups; 2. Known pregnant or lactating women; 3. Unable to sign the informed consent form; 4. The researcher determines other circumstances that are not suitable for inclusion in the study.

Design outcomes

Primary

MeasureTime frame
Real-World Progression-Free Survival (rwPFS);Overall Survival (OS);Time to Treatment Failure (TTF);Time to First Subsequent Therapy or Death (TFST);

Countries

China

Contacts

Public ContactXudong Hu

Shandong First Medical University and Shandong Academy of Medical Sciences (Shandong Cancer Hospital &Institute)

drhuxudong@163.com+86 531 67626418

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026