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Efficacy and safety of Iruplinalkib in real-world patients with ALK-positive and ROS1-positive NSCLC

Efficacy and safety of Iruplinalkib in real-world patients with ALK-positive and ROS1-positive NSCLC

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400092150
Enrollment
Unknown
Registered
2024-11-11
Start date
2024-11-11
Completion date
Unknown
Last updated
2024-11-18

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

Conditions

NSCLC

Interventions

Experimental group:Iruplinalkib

Sponsors

Second Hospital of Shanxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Sign informed consent and join the study voluntarily; 2. Pathological diagnosis of ALK positive or ROS1 positive NSCLC; 3. age =18 years old; 4. no targeted therapy contraindications; 5. The investigator judged that Iruak therapy (either monotherapy or combination therapy) was acceptable.

Exclusion criteria

Exclusion criteria: 1.A positive baseline pregnancy test for pregnant, lactating or fertile women; 2.Pulmonary interstitial disease, drug-related pneumonia or other radiation pneumonia that still requires drug intervention; 3.Proven allergy to Iruak and its excipients;

Design outcomes

Primary

MeasureTime frame
Adverse Events;

Secondary

MeasureTime frame
Overall Survival;Progression-free survival;Objective Response Rate;Disease Control Rate;

Countries

China

Contacts

Public ContactSong Xiang

Second Hospital of Shanxi Medical University

songxiangeryuan@163.com+86 138 0343 6909

Outcome results

None listed

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