Analyst Makes Prescient Call Ahead Of Celgene Disappointments


Shares of Celgene (CELG) are plunging after the company slashed its 2020 sales guidance. This follows last week’s announcement that the biotech company is discontinuing a late-stage Crohn’s treatment trial. Back on October 5, and ahead of both negative events, Morgan Stanley analyst Matthew Harrison had downgraded Celgene to Underweight, citing underappreciated generic risk and a cautious view on its 2018 pipeline potential.

RESULTS, DISCONTINUATION: This morning, Celgene reported third quarter adjusted earnings per share of $1.91, which was above consensus of $1.87. The company also announced third quarter revenue of $3.29B, below consensus of $3.42B. Meanwhile, the said it sees 2017 adjusted earnings per share of $7.30-$7.35, and lowered its 2017 total revenue forecast to approximately $13B from a prior view of $13B-$13.4B. Additionally, the company said it sees 2020 adjusted earnings per share greater than $12.50 versus previous view of greater than $13.00, while cutting its total 2020 net product sales outlook to $19B-$20B from over $21B. This comes a week after the company announced that the GED-0301 phase III REVOLVE trial in Crohn’s disease and the extension trial will be discontinued. Celgene has decided to stop the trials following an October recommendation of the Data Monitoring Committee, which assessed overall benefit/risk during a recent interim futility analysis. There were no meaningful safety imbalances identified in the analysis. The company added that it is waiting to review the full dataset from the phase II trial with GED-0301 in ulcerative colitis to determine next steps.

SELL CELGENE: On October 5, Morgan Stanley’s Harrison downgraded Celgene to Underweight saying consensus underappreciated the potential for generic Revlimid as early as April 2020, much sooner that the expected 2026 entry, and the challenges key pipeline assets GED-0301 and ozanimod could face. The analyst noted that Dr. Reddy’s (RDY) has a unique polymorph of Revlimid as revealed by an EU patent filling, and expects it to file a inter partes review, or IPR, by October 2020.

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