Meanwhile, the company reported a net narrower loss of $71.4 million, or $2.28 per share, compared to $75.2 million, or $2.58 per share in the prior year quarter. Analysts had projected a wider loss of $2.60 per share.
The New York-based biotech did not change its 2019 Ocaliva net sales guidance range, which was projected between $235 million and $245 million. Guidance for adjusted operating expenses was also kept unchanged in the range of $470 million to $500 million.
READ: What is NASH and which biotech firms are vying for the first-mover status
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Intercept shares ended their last trading session up 3.36% on Tuesday. ICPT stock is down 50% in the past four months, after the company reported some side effects including itching for Ocaliva when used in the treatment for NASH (nonalcoholic steatohepatitis), despite positive data from phase 3 trials.
Though Ocaliva is the most advanced drug being tested for this liver disease, investors remained cautious as rival Gilead Sciences’ (NASDAQ: GILD) phase 2 NASH candidate does not report these side-effects.
READ: Intercept stock surges on positive data from liver fibrosis drug study
Gilead’s own most advanced NASH candidate selonsertib had
earlier this year failed
in the Phase 3 efficacy tests.
Executive Vice President of Intercept’s Research &
Development said, “As the only Phase 3 study currently being conducted in this
more advanced segment of the NASH population, we’ve been pleased with the
strong momentum we’ve seen in screening and randomization rates, and even after
expanding REVERSE, remain on track to complete target enrollment this year.