Skip to content

DYNAMIC ” IDentifY the best therapeutic sequeNcing strAtegy in oncogene addICted NSCLC:” “A multi-arms prospective, randomized phase II study to evaluate the best sequential therapeutic strategis in patients with metastatic non-small cell lung cancer harboring targetable genomic driver alterations”

Status
Not yet recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2026-525268-16-00
Enrollment
962
Registered
2026-10-19
Start date
Unknown
Completion date
Unknown
Last updated
2026-10-19

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

Conditions

Non Small Cell Lung Cancer

Brief summary

PFS2 at two years is the primary endpoint of the study

Detailed description

OS, ORR, DoR, TRAEs, HRQoL

Interventions

DRUGLazcluze 240 mg film-coated tablets
DRUGOPDIVO 300 mg solution for injection
DRUGLIBTAYO 350 mg concentrate for solution for infusion.
DRUGOSIMERTINIB
DRUGTecentriq 1 200 mg concentrate for solution for infusion
DRUGYERVOY 5 mg/ml concentrate for solution for infusion
DRUGLazcluze 80 mg film-coated tablets
DRUGPaclitaxel Fresenius Kabi 6 mg/ml koncentrat till infusionsvätska
DRUGlösning
DRUGMektovi 45 mg film-coated tablets
DRUGRybrevant 1600 mg solution for injection
DRUGCisplatin Sandoz 0
DRUG5 mg/ml koncentrátum oldatos infúzióhoz
DRUGRybrevant 2240 mg solution for injection
DRUGKEYTRUDA 25 mg/mL concentrate for solution for infusion.
DRUGKRAZATI 200 mg film-coated tablets
DRUGOPDIVO 10 mg/mL concentrate for solution for infusion.
DRUGCarboplatin Pfizer 450 mg Konzentrat zur Infusionsbereitung
DRUGPemetrexed EVER Pharma 25 mg/ml koncentrat till infusionsvätska

Sponsors

Universita' Degli Studi Di Torino
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
PFS2 at two years is the primary endpoint of the study—

Secondary

MeasureTime frame
OS, ORR, DoR, TRAEs, HRQoL—

Outcome results

None listed

Source: EU CTIS · Data processed: Oct 20, 2026