Biohaven shares hold Overweight rating on clinical trial success

Published 23/09/2024, 16:34
Biohaven shares hold Overweight rating on clinical trial success


On Monday, Piper Sandler maintained a positive stance on Biohaven Pharmaceutical Holding (NYSE:BHVN) shares, reiterating an Overweight rating with a price target of $76.00. This affirmation follows the unexpected success of Biohaven's troriluzole in Spinocerebellar Ataxia (SCA) clinical trials.

The analyst highlighted the significant turnaround for troriluzole, a drug that had previously seen multiple Phase 3 trial failures and a Refusal to File (RTF) from the FDA. The recent trial results showed statistically significant improvements over natural history controls on the primary endpoint at the first, second, and third year marks, along with similar improvements across nine secondary endpoints.

The positive trial outcomes, coupled with indications that the FDA is receptive to the new data, have led to the expectation of a New Drug Application (NDA) filing in the next quarter. The analyst anticipates a potential market launch next year with projected U.S. revenues reaching $250 million by 2030.

Piper Sandler's valuation method has been adjusted to account for the newfound potential of troriluzole in treating SCA, a factor that was previously dismissed by many investors. The firm's current price target suggests confidence in the drug's commercial prospects and its contribution to Biohaven's growth.

In other recent news, Biohaven Pharmaceutical Holding Company plans to submit a New Drug Application to the FDA for troriluzole in the fourth quarter of 2024, anticipating potential commercialization in 2025.

In relation to Biohaven's financial arrangements, the company has filed a prospectus supplement for the resale of approximately 1.8 million common shares by a significant shareholder. Moving on to analysts' insights, Jefferies and Bernstein SocGen Group have initiated coverage on Biohaven with a Buy and Outperform rating respectively, emphasizing the potential of the company's diverse portfolio.

Lastly, the company has received FDA approval for Multiple Ascending Dose studies in Rheumatoid Arthritis patients for its lead candidate BHV-1300. These recent developments underline Biohaven's ongoing commitment to its drug development programs.


InvestingPro Insights


As Biohaven Pharmaceutical (NYSE:BHVN) garners positive attention following its clinical trial success, InvestingPro data provides a deeper financial perspective on the company. Currently, Biohaven holds a market capitalization of $3.82 billion, indicative of its substantial size within the biopharmaceutical market.

Despite the optimism surrounding its drug troriluzole, the company's P/E ratio stands at -4.13, reflecting investor concerns about profitability, with analysts not expecting the company to be profitable this year. This is further highlighted by an adjusted P/E ratio for the last twelve months as of Q2 2024 at -5.01.

However, there are bright spots in the company's financial health. Biohaven holds more cash than debt on its balance sheet, suggesting a strong liquidity position. This is further supported by the fact that liquid assets exceed short-term obligations.

Moreover, two analysts have revised their earnings upwards for the upcoming period, indicating potential optimism in the company's financial trajectory. Biohaven has demonstrated a high return over the last year, with a 138.57% price total return, showcasing its strong market performance in the recent period.

InvestingPro Tips reveal that while Biohaven faces challenges with weak gross profit margins and an anticipated drop in net income, it has also seen a strong return over the last three months, with a 20.35% price total return. It is worth noting that Biohaven does not pay a dividend, which may be a consideration for income-focused investors. For those seeking a comprehensive analysis and additional insights, InvestingPro offers further tips on Biohaven, available at: https://www.investing.com/pro/BHVN.

This article was generated with the support of AI and reviewed by an editor. For more information see our T&C.

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