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NPT-2042

Alternative Names: NPT-2042, NPT 2042, NPT2042
Latest Update: 2024-08-28
Latest Update Note: Clinical Trial Update

Product Description

An orally administered adjunct treatment option for epilepsy patients who lack seizure control or who are unable to tolerate the side effects of their currently prescribed therapies. The primary objective of the Phase 2 study is to assess the efficacy of NPT 2042 compared with placebo as an adjunctive treatment for focal-onset epilepsy. (Sourced from: https://neuropro.io/providers/)

Mechanisms of Action: Unknown

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: N/A

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: NeuroPro Therapeutics, Inc.
Company Location:
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for NPT-2042

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

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