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Piper Sandler sees Praxis stock gaining momentum with upcoming Phase 2 and Phase 3 results

EditorAhmed Abdulazez Abdulkadir
Published 12/11/2024, 12:27 PM
PRAX
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On Wednesday, Piper Sandler reaffirmed its Overweight rating on shares of Praxis Precision Medicines Inc. (NASDAQ:PRAX) with a consistent price target of $270.00. The company, now valued at $1.3 billion, has seen its stock surge over 213% year-to-date, making it one of the strongest performers in the biotech sector.

According to InvestingPro data, analyst targets range from $57 to $270, reflecting diverse views on the company's potential. The firm's optimism is rooted in the potential of Praxis's pipeline, including the ulixacaltamide's Phase 3 Essential3 ET Study 1 interim results expected in the first quarter of 2025, as well as other promising drugs in development.

A recent fireside chat with Praxis provided insights into several key aspects of the company's drug development efforts. The discussion covered the anticipated scenarios for ulixacaltamide's interim study results, the drug's potential in treating Parkinson's disease, and the development of vormatrigine for focal onset seizures/generalized epilepsy.

While the company maintains a strong liquidity position with a current ratio of 10.96 and more cash than debt on its balance sheet, InvestingPro analysis indicates the company is not yet profitable, with analysts expecting continued losses this year. Additionally, the conversation touched upon relutrigine's Phase 2 EMBOLD Cohort 2 progress in treating SCN2A/SCN8A developmental and epileptic encephalopathies.

Piper Sandler also hosted an investor dinner where further details regarding the Essential3 Study 1 interim analysis were discussed. The event highlighted the robust interest from participants and reinforced the significant market opportunity for treating essential tremor, which affects an estimated 2 million patients in the United States.

The analyst note from Piper Sandler captures Praxis's commentary on their other pipeline assets. The company has set expectations for vormatrigine's Phase 2 RADIANT study results in the first half of 2025 and reported that relutrigine Cohort 2 is progressing well.

In conclusion, Piper Sandler's stance on Praxis Precision Medicines remains positive, with the expectation that 2025 will be a pivotal year for the company to drive substantial gains in its share value. With a strong analyst consensus rating of 1.5 (where 1 is Strong Buy), the market appears optimistic about Praxis's future.

Discover 14 additional key insights about PRAX and access comprehensive financial analysis with InvestingPro.

In other recent news, Praxis Precision Medicines has seen a surge in analyst confidence, with Jefferies raising the company's target to $305 from $144, Piper Sandler maintaining its Overweight rating and $270.00 price target, and Guggenheim keeping its Buy rating with a $170 target. These ratings reflect the promising developments in Praxis's neurology-focused assets, particularly ulixa for essential tremor treatment, vormatrigine for focal and generalized epilepsy, and relutrigine for developmental and epileptic encephalopathies (DEE).

Praxis is expected to release Phase 3 interim results for ulixa and open-label Phase 2 data for vormatrigine within the first half of 2025. Registrational data for relutrigine is anticipated in the first half of 2026. The company's recent decision to enhance executive severance terms underscores its commitment to retaining top leadership.

Praxis's drug candidate, Relutrigine, demonstrated a significant 46% reduction in motor seizures in a Phase 2 study, with over 30% of patients achieving freedom from seizures. These developments in Praxis's research and development efforts have been positively received by various analyst firms.

Oppenheimer maintained its Outperform rating and a price target of $143, following the news of Lundbeck's acquisition of Longboard Pharmaceuticals, seen as a positive reflection on the DEE therapeutic area.

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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