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Lisdexamfetamine

Alternative Names: lisdexamfetamine, vyvanse, lisdexamphetamine, nrp104, elvanse
Latest Update: 2024-11-28
Latest Update Note: Clinical Trial Update

Product Description

Mechanisms of Action: DRI Inhibitor

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: Australia | Austria | Belgium | Brazil | Canada | Chile | Colombia | Denmark | Dominican Republic | Estonia | Finland | Germany | Hong Kong | Iceland | Ireland | Israel | Japan | Lithuania | Mexico | Netherlands | New Zealand | Norway | Poland | Portugal | Romania | Singapore | South Africa | Spain | Sweden | Switzerland | United Kingdom | United States

Approved Indications: Binge-Eating Disorder | Attention Deficit Disorder with Hyperactivity

Known Adverse Events: Attention Deficit Disorder with Hyperactivity | Abdominal Pain | Dizziness | Pain Unspecified | Insomnia | Anorexia | Constipation | Diarrhea

Company: None
Company Location:
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Lisdexamfetamine

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Recent News Events

Date

Type

Title

11/18/2024

News Article

 Elite Pharmaceuticals Receives FDA Approval for Generic Vyvanse

10/31/2024

News Article

 Takeda Announces Strong First Half FY2024 Results and Raises Full Year Outlook

09/23/2024

News Article

 New Study Warns of High Dose "ADHD" Drugs Inducing Psychosis

07/31/2024

News Article

 Takeda Announces First Quarter FY2024 Results - Strong Performance by Growth & Launch Products; Advancements in Promising Late-Stage Pipeline

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