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Study of Treatment High Risk and/or Low Risk Acute Lymphoblastic leukémia(ALL) Adults Stage III

F

French Innovative Leukemia Organisation

Status and phase

Completed
Phase 3

Conditions

Leukemia, Lymphocytic, Acute

Treatments

Drug: interferon alpha 2a

Study type

Interventional

Funder types

Other

Identifiers

NCT00483132
GOELAL02

Details and patient eligibility

About

Improved outcome of high risk lymphoblastic leukemia (ALL) with laite high dose therapy.

High dose versus conventional therapy for adult low risk T-ALL and Lymphoblastic lymphoma (LBL).

Full description

Comparison between two autograf therapeutic strategies in high risk patients Ramdomised comparison between maintenance treatment with or not interferon alpha 2 a

Enrollment

232 patients

Sex

All

Ages

15 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria

  • ALL high risk or low risk or lymphoblastic lymphoma
  • age 15-55 years old
  • informed consent signed

Exclusion Criteria:

  • patients previously treated with a chemotherapy or alpha-interferon
  • ALL 3 (burkitt like)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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