Deutsche Bank raises Harmony Biosciences Hldgs target to $36

0 min read     Updated on 01 Jul 2026, 01:02 AM
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Radhika SScanX News Team
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Deutsche Bank maintains a Hold rating on Harmony Biosciences Hldgs and raises the price target to $36 from $30.

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Deutsche Bank analyst David Hoang has maintained a Hold rating on Harmony Biosciences Hldgs while adjusting the stock's price target upward. The new target is set at $36, an increase from the previous $30. The company's shares trade on the NASDAQ under the ticker HRMY.

The revised target reflects an updated valuation perspective from the financial institution. Harmony Biosciences Hldgs operates within the biotechnology sector, focusing on therapeutic solutions.

Rating Action Previous Target New Target
Hold $30 $36

What specific factors drove Deutsche Bank to revise the valuation upward while maintaining a Hold rating?

How might this price target adjustment influence investor sentiment toward Harmony Biosciences in the short term?

What upcoming clinical or regulatory milestones could further impact the stock's performance?

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Harmony Biosciences to present six posters at SLEEP 2026

1 min read     Updated on 11 Jun 2026, 05:49 PM
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Harmony Biosciences Holdings, Inc. announced six poster presentations on narcolepsy and idiopathic hypersomnia at the SLEEP 2026 annual meeting in Baltimore from June 14–17. The presentations include data on Pitolisant, HBS-301, and HBS-201 from various clinical trial phases.

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Harmony Biosciences Holdings, Inc. will present six abstracts focused on narcolepsy and idiopathic hypersomnia at SLEEP 2026, the 40th annual meeting of the Associated Professional Sleep Societies (APSS). The event is scheduled to take place in Baltimore, MD, from June 14 to June 17. The presentations will include data on treatments such as Pitolisant, HBS-301, and HBS-201, reflecting the company's ongoing research in rare neurological diseases.

The accepted abstracts include a pooled analysis of Pitolisant treatment in adults with narcolepsy and an analysis of Phase 3 trial sleep diary data regarding the drug's effect on sleep patterns in idiopathic hypersomnia. Additionally, the company will present findings from Phase 3, randomized, double-blind, placebo-controlled studies of HBS-301 for both narcolepsy and idiopathic hypersomnia.

Further presentations will detail results from a Phase 1b clinical trial on the dosing optimization of the Pitolisant gastro-resistant formulation (HBS-201) in adults with narcolepsy. A cross-sectional study regarding patient experience of fatigue and assessment in narcolepsy is also on the agenda. The final poster will cover the long-term safety and effectiveness of Pitolisant in adult patients with idiopathic hypersomnia, presenting final results from an open-label Phase 3 trial.

Presentation Schedule

Abstract Title Poster Presentation Session
Treatment with Pitolisant in Subgroups of Adults with Narcolepsy: Pooled Analysis of Two Randomized Clinical Trials P-16 (Poster #387), 6/15/2026, 10:00-10:45 a.m.
Effect of Pitolisant on Sleep Patterns in Idiopathic Hypersomnia: Analysis of Phase 3 Trial Sleep Diary Data P-16 (Poster #378), 6/15/2026, 11:00-11:45 a.m.
Phase 3, Randomized, Double-Blind, Placebo-Controlled Studies of HBS-301 for Narcolepsy and Idiopathic Hypersomnia P-1 (Poster #384), 6/15/2026, 11:00-11:45 a.m.
Pitolisant Gastro-Resistant Formulation (HBS-201) Dosing Optimization Study in Adults with Narcolepsy: Results from a Phase 1b Clinical Trial P-41 (Poster #525), 6/16/2026, 10:00-10:45 a.m.
Patient Experience of Fatigue and Assessment in Narcolepsy: A Cross-Sectional Study P-35 (Poster #330), 6/16/2026, 11:00-11:45 a.m.
Long-Term Safety and Effectiveness of Pitolisant in Adult Patients with Idiopathic Hypersomnia: Final Results From an Open-Label Phase 3 Trial P-41 (Poster #524), 6/16/2026, 11:00-11:45 a.m.

Harmony Biosciences is a pharmaceutical company dedicated to developing and commercializing innovative therapies for patients with rare neurological diseases who have unmet medical needs. The company was established by Paragon Biosciences, LLC, in 2017 and is headquartered in Plymouth Meeting, Pa.

What are the potential regulatory timelines for HBS-301 following the presentation of Phase 3 data?

How might the optimized dosing of HBS-201 improve patient adherence compared to current formulations?

Could the long-term safety data for Pitolisant in idiopathic hypersomnia support label expansions?

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