Brief: AB Science Gets FDA Authorisation For New Trial In Leukemia
Nov 22 (Reuters) - AB SCIENCE SA ABS.PA :
* AB SCIENCE RECEIVED FDA AUTHORIZATION TO INITIATE PHASE
1/II
TRIAL OF AB8939 IN THE TREATMENT OF ACUTE MYELOID LEUKEMIA
* STUDY AB18001 HAS ALSO BEEN APPROVED IN FRANCE AND IN
CANADA
* AB8939 WAS GRANTED ORPHAN DRUG DESIGNATION FOR AML FROM
U.S.
FOOD AND DRUG ADMINISTRATION (FDA)
* THE ESTIMATED TARGETED POPULATION OF AB8938 IN AML IS
AROUND
80,000 PEOPLE IN EUROPE AND THE US
Source text for Eikon: ID:nGNE4DkzpJ
Further company coverage: ABS.PA
(Gdansk Newsroom)
((gdansk.newsroom@thomsonreuters.com; +48 58 7696600;))
Recent news on AB Science SA
See all newsBrief: AB Science Temporarily Halts Europe Clinical Trials Ahead Of Strategic Reorganization
Brief: AB Science Says FDA Granted Status Of Minor Use In Major Species For Masivet
Brief: AB Science Says Co Received Japanese Patent Protection To Use Masitinib In Progressive MS Until 2041
Brief: AB Science Phase 1 AML Study Of AB8939 Shows 100% Partial Response Rate
Brief: AB Science Receives Notice Of Allowance For European Patent Covering Masitinib Until 2040 In Treatment Of Sickle Cell Disease