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Fospropofol

Alternative Names: fospropofol, lusedra
Latest Update: 2024-12-13
Latest Update Note: Clinical Trial Update

Product Description

Fospropofol (FP), also known as GPI15715 or Aquavan, is a new molecular entity with sedative-hypnotic properties, to be administered intravenously and proposed for the indication of sedation in adult patients undergoing diagnostic or therapeutic procedures. (Sourced from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3487287/)

Mechanisms of Action: GABA Agonist

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Intravenous

FDA Designation: None *

Approval Status: Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Eisai
Company Location: BUNKYO-KU TOKOYO 112 M0
Company CEO: Haruo Naito
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Fospropofol

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 4: Anesthesia Related|Bradycardia|Hypotension|Tremor|Pain Unspecified|Other

Phase 3: Carpal Tunnel Syndrome|Bunion|Pain Unspecified|Nasal Polyposis|Shoulder Pain|Pain, Referred

Phase 2: Pain Unspecified|Hypotension|Other

Phase 1: Anesthesia Related|Pregnancy Outcomes|Drug Hypersensitivity

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

ChiCTR2400092104

N/A

Not yet recruiting

Anesthesia Related

2027-10-15

ChiCTR2400093011

N/A

Not yet recruiting

Paresthesia|Resistant Hypertension|Tachycardia|Stroke|Bradycardia|Hypotension

2027-08-31

ChiCTR2400085355

N/A

Not yet recruiting

Hepatic Insufficiency

2027-06-10

XWANG

P4

Not yet recruiting

Tremor|Bradycardia|Hypotension

2027-05-31

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