SymbolZVRA
NameZEVRA THERAPEUTICS, INC.
SectorHEALTH CARE
RegionNorth America
IndustryBiotechnology: Pharmaceutical Preparations
Address1180 CELEBRATION BOULEVARD,SUITE 103, CELEBRATION, Florida, 34747, United States
Telephone+1 321 939-3416
Fax
Email
Websitehttps://www.zevra.com
IncorporationUNDEFINED
Incorporated On
Employees
Fiscal Year
Public Since
ExchangesNASDAQ
Auditor
Audit StatusNOT PROVIDED
Reporting Status
CIK0001434647
Description

Zevra Therapeutics, Inc. is a rare disease therapeutics company. The Company is engaged in creating therapies for diseases with limited or no treatment options. The Company has a diverse portfolio of products and product candidates, which includes a combination of both a clinical-stage pipeline and commercial stage assets. It employs its LAT platform technology to create a portfolio of approved products. Its product candidates include Arimoclomol, KP1077IH, KP1077N and AZSTARYS. Arimoclomol is an orally delivered, investigational product candidate being developed for Niemann-Pick disease type C (NPC). KP1077 is the Companys lead clinical development product candidate, which is being developed as a treatment for idiopathic hypersomnia (IH) and narcolepsy. KP1077 is comprised solely of serdexmethylphenidate (SDX), the Companys prodrug of d-methylphenidate (d-MPH). AZSTARYS is a prodrug for the treatment of ADHD in patients aged six years or older.

Additional info from NASDAQ:
Zevra Therapeutics, Inc. is a rare disease therapeutics company. The Company is engaged in creating therapies for diseases with limited or no treatment options. The Company has a diverse portfolio of products and product candidates, which includes a combination of both a clinical-stage pipeline and commercial stage assets. It employs its LAT platform technology to create a portfolio of approved products. Its product candidates include Arimoclomol, KP1077IH, KP1077N and AZSTARYS. Arimoclomol is an orally delivered, investigational product candidate being developed for Niemann-Pick disease type C (NPC). KP1077 is the Companys lead clinical development product candidate, which is being developed as a treatment for idiopathic hypersomnia (IH) and narcolepsy. KP1077 is comprised solely of serdexmethylphenidate (SDX), the Companys prodrug of d-methylphenidate (d-MPH). AZSTARYS is a prodrug for the treatment of ADHD in patients aged six years or older.

2026-08-17 20:32

Thompson Rahsaan 🔴 sold 42.7K shares of ZEVRA THERAPEUTICS, INC. (ZVRA) at $11.13 Transaction Date: Aug 14, 2026 | Filing ID: 000073

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2026-08-14 20:31

📋 RAHSAAN THOMPSON (Officer) plans to sell 43K shares of ZEVRA THERAPEUTICS INC (at $11.18 each, total $477K) Filed: Aug 14, 2026 | ID: 008134

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2026-08-14 12:07

New Form SCHEDULE 13G/A - ZEVRA THERAPEUTICS, INC. <b>Filed:</b> 2026-08-14 <b>AccNo:</b> 0000919574-26-005266 <b>Size:</b> 9 KB

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2026-08-13 14:00

INVESTOR ALERT: Pomerantz Law Firm Investigates Claims On Behalf of Investors of Zevra Therapeutics, Inc. - ZVRA

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2026-08-12 20:16

Director Watton Corey Michael 🟡 adjusted position in 12.3K shares (1 derivative) of ZEVRA THERAPEUTICS, INC. (ZVRA) at $11.25 Transaction Date: Aug 10, 2026 | Filing ID: 000070

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2026-08-07 03:02

INVESTOR ALERT: Pomerantz Law Firm Investigates Claims On Behalf of Investors of Zevra Therapeutics, Inc. - ZVRA

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2026-08-04 11:30

Zevra Therapeutics to Present at the Canaccord Genuity Annual Growth Conference

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2026-08-03 11:30

Zevra Therapeutics Announces Publication of Four-Year Real-World Data from U.S. Early Access Program Evaluating MIPLYFFA® (arimoclomol) in Niemann-Pick Disease Type C (NPC)

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2026-07-31 11:51

New Form SCHEDULE 13G - ZEVRA THERAPEUTICS, INC. <b>Filed:</b> 2026-07-31 <b>AccNo:</b> 0002100119-26-001518 <b>Size:</b> 7 KB

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2026-07-30 14:00

INVESTOR ALERT: Pomerantz Law Firm Investigates Claims On Behalf of Investors of Zevra Therapeutics, Inc. - ZVRA

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Trial ID Title Phase Indication Status Start Date Completion Date Source
NCT07125066 An Individual Patient, Open Label Study to Use ACER-001 to Treat Combined D,L-2… Phase1 Combined D,L-2-hydroxyglutaric Aciduria Enrolling_By_Invitation 2025-07-30 2027-12-01 ClinicalTrials.gov
NCT06773026 Study of Sodium Phenylbutyrate (ACER-001) for the Treatment of Pediatric and Ad… Phase2 Medium-chain Acyl-CoA Dehydrogenase Deficiency Recruiting 2025-06-30 2027-07-01 ClinicalTrials.gov
NCT05668754 Study of SDX in Patients With Idiopathic Hypersomnia (IH) Phase2 Idiopathic Hypersomnia Completed 2022-12-28 2024-03-21 ClinicalTrials.gov
NCT03460652 KP415 Open-Label Safety Study in Children (6-12 Years of Age) With ADHD Phase3 ADHD Completed 2018-03-13 2019-07-09 ClinicalTrials.gov
NCT03292952 KP415 Classroom Study in Children (6-12 Years of Age) With ADHD Phase3 ADHD Completed 2017-12-20 2018-05-16 ClinicalTrials.gov
Total clinical trials: 5
Product Name Type Development Stage Therapeutic Area Study Status Trial ID
Placebo Other Phase PHASE2 Idiopathic Hypersomnia COMPLETED NCT05668754
Serdexmethylphenidate Other Phase PHASE2 Idiopathic Hypersomnia COMPLETED NCT05668754
Sodium phenylbutyrate Other Phase PHASE1 Combined D,L-2-hydroxyglutaric Aciduria ENROLLING_BY_INVITATION NCT07125066
Sodium phenylbutyrate Other Phase PHASE2 Medium-chain Acyl-CoA Dehydrogenase Deficiency RECRUITING NCT06773026
KP415 oral capsule Other Phase PHASE3 ADHD COMPLETED NCT03460652
Placebo oral capsule Other Phase PHASE3 ADHD COMPLETED NCT03292952
KP415 oral capsule Other Phase PHASE3 ADHD COMPLETED NCT03292952
Placebo Other Phase PHASE2 Idiopathic Hypersomnia COMPLETED NCT05668754
Serdexmethylphenidate Other Phase PHASE2 Idiopathic Hypersomnia COMPLETED NCT05668754
Sodium phenylbutyrate Other Phase PHASE2 Medium-chain Acyl-CoA Dehydrogenase Deficiency RECRUITING NCT06773026
Sodium phenylbutyrate Other Phase PHASE1 Combined D,L-2-hydroxyglutaric Aciduria ENROLLING_BY_INVITATION NCT07125066
Total products: 11