** BTIG sees attractive opportunity in gene therapy after
recent weakness due to FDA scrutiny and safety concerns
** Brokerage says FDA approvals for Luxturna and Zolgensma
gene therapies, M&A activities, and efficacy readouts suggest
the potential of transformative therapies
** In 2019, the U.S. FDA approved Zolgensma, Novartis'
NOVN.S gene therapy for spinal muscular atrophy (SMA); in
2017, the FDA said Spark Therapeutics Inc's experimental gene
therapy, Luxturna, for a rare inherited form of blindness is
effective
** "Better understanding of human biology and continued
innovation in technology should support even accelerated
translation from the lab to the clinic" - BTIG
** Says increase in clinical holds reflects increasing
clinical development activities in gene therapy; believes FDA is
comfortable with safety in gene therapy
** "Disorders that affect the central nervous system (CNS)
represents a significant potential for gene therapy" - BTIG
** BTIG initiates coverage on the following cos:
Company RIC Rating PT
Applied Genetic AGTC.O Buy $11
Technologies
AVROBIO AVRO.O Buy $23
Magenta Therapeutics MGTA.O Buy $20
Passage Bio PASG.O Buy $25
Sarepta Therapeutics SRPT.O Buy $110
Selecta Biosciences SELB.O Buy $10
Sio Gene Therapies SIOX.O Buy $8
Taysha Therapeutics TSHA.O Buy $44
Uniqure QURE.O Buy $46
(Reporting by Siddarth S)
((Siddarth.s@thomsonreuters.com;))