Scemblix® (Asciminib): Prospective Non Interventional Study as 3rd Line Therapy or More to Treat Adult Patients With CML-CP in Real World Setting in France

Status: Recruiting
Location: See all (38) locations...
Intervention Type: Other
Study Type: Observational
SUMMARY

The purpose of this study is to enhance the knowledge on asciminib treatment in a broader and real-life population by collecting additional data to characterize the treatment patterns of patients treated with asciminib, with a primary objective represented by maintenance on treatment at 12 months.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 99
Healthy Volunteers: f
View:

• Patient aged ≥ 18 years at inclusion,

• Patient with Ph+ CML-CP previously treated with two or more TKIs,

• Patient for whom a decision has been taken by the treating physician (investigator) to initiate treatment with asciminib according to his own practice, the drug label / Summary of Product Characteristics (SmPC), and regardless of study participation,

• Patient having given their non objection to participate to the study

Locations
Other Locations
France
Novartis Investigative Site
RECRUITING
Aix-en-provence
Novartis Investigative Site
RECRUITING
Amiens
Novartis Investigative Site
RECRUITING
Angers
Novartis Investigative Site
RECRUITING
Antibes
Novartis Investigative Site
RECRUITING
Avignon
Novartis Investigative Site
RECRUITING
Besançon
Novartis Investigative Site
RECRUITING
Bordeaux
Novartis Investigative Site
RECRUITING
Bordeaux
Novartis Investigative Site
RECRUITING
Brest
Novartis Investigative Site
RECRUITING
Brive-la-gaillarde
Novartis Investigative Site
RECRUITING
Caen
Novartis Investigative Site
ACTIVE_NOT_RECRUITING
Cagnes-sur-mer
Novartis Investigative Site
RECRUITING
Cannes
Novartis Investigative Site
RECRUITING
Challes-les-eaux
Novartis Investigative Site
RECRUITING
Dunkirk
Novartis Investigative Site
RECRUITING
Grenoble
Novartis Investigative Site
WITHDRAWN
Le Mans
Novartis Investigative Site
RECRUITING
Lens
Novartis Investigative Site
ACTIVE_NOT_RECRUITING
Libourne
Novartis Investigative Site
ACTIVE_NOT_RECRUITING
Lyon
Novartis Investigative Site
RECRUITING
Montpellier
Novartis Investigative Site
RECRUITING
Montpellier
Novartis Investigative Site
RECRUITING
Mulhouse
Novartis Investigative Site
RECRUITING
Nice
Novartis Investigative Site
RECRUITING
Nîmes
Novartis Investigative Site
RECRUITING
Orléans
Novartis Investigative Site
RECRUITING
Périgueux
Novartis Investigative Site
RECRUITING
Quimper
Novartis Investigative Site
RECRUITING
Rennes
Novartis Investigative Site
RECRUITING
Saint Priest En Jarez
Novartis Investigative Site
RECRUITING
St-malo
Novartis Investigative Site
RECRUITING
Strasbourg
Novartis Investigative Site
RECRUITING
Tarbes
Novartis Investigative Site
RECRUITING
Tours
Novartis Investigative Site
RECRUITING
Trévenans
Novartis Investigative Site
RECRUITING
Troyes
Novartis Investigative Site
RECRUITING
Valence
Novartis Investigative Site
RECRUITING
Vesoul
Contact Information
Primary
Novartis Pharmaceuticals
novartis.email@novartis.com
+41613241111
Backup
Novartis Pharmaceuticals
Time Frame
Start Date: 2024-03-06
Estimated Completion Date: 2026-12-15
Participants
Target number of participants: 168
Treatments
Asciminib
Adult patients with Ph+ CML-CP previously treated with two or more tyrosine kinase inhibitors
Sponsors
Leads: Novartis Pharmaceuticals

This content was sourced from clinicaltrials.gov

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