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Continuation of Drug Supply in Chinese Patients After CAMN107DBR01study Termination (MACS2226)

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Novartis

Status

Conditions

Gastrointestinal Stromal Tumor

Treatments

Drug: Glivec

Study type

Expanded Access

Funder types

Industry

Identifiers

NCT01613053
CAMN107DCN03

Details and patient eligibility

About

Continuation of drug supply in Chinese patients after CAMN107DBR01study termination.

Full 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.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Five patients who are on treatment of imatinib and deriving clinical benefit after CAMN107DBR01 study termination and written informed consent obtained.

Exclusion criteria

  • N/A.

Trial contacts and locations

3

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Data sourced from clinicaltrials.gov

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