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No Longer AvailableNCT01613053

Continuation of Drug Supply in Chinese Patients After CAMN107DBR01study Termination

Status
No Longer Available
Phase
Study type
Expanded Access
Enrollment
Sponsor
Novartis Pharmaceuticals · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Continuation of drug supply in Chinese patients after CAMN107DBR01study termination.

Detailed description

Five patients who are on treatment of imatinib and deriving clinical benefit after CAMN107DBR01 study termination and written informed consent obtained will enter the trial, all five patients will receive Glivec (8oomg per day) treatment until tumor progression \[by RECIST guidelines, version 1.0\], unacceptable toxicity, death or withdrawal of consent.

Conditions

Interventions

TypeNameDescription
DRUGGlivec800 mg per day

Timeline

First posted
2012-06-06
Last updated
2015-04-24

Locations

3 sites across 1 country: China

Source: ClinicalTrials.gov record NCT01613053. Inclusion in this directory is not an endorsement.