Aug 1 (Reuters) - Hansa Biopharma AB HNSA.ST:
HANSA BIOPHARMA ANNOUNCES SUPPORTIVE DATA FROM TREATMENT WITH IMLIFIDASE PRIOR TO THE ADMINISTRATION OF GENE THERAPY FOR DUCHENNE MUSCULAR DYSTROPHY
BASED ON THESE OUTCOMES, HANSA AND SAREPTA WILL DISCUSS APPROPRIATE NEXT STEPS FOR PROGRAM.
SAFETY PROFILE OF IMLIFIDASE WAS IN KEEPING WITH PRIOR EXPERIENCE AND THE TRIAL DID NOT GENERATE ANY NEW SAFETY SIGNALS
HANSA-12 WEEKS AFTER ADMINISTRATION OF GENE THERAPY, PATIENTS IN TRIAL DEMONSTRATED EVIDENCE OF AAV-MEDIATED TRANSDUCTION, EXPRESSION OF MICRO-DYSTROPHIN
Source text: ID:nWkr1lhBGB
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