Single & Multiple Ascending Dose Safety Study of XPF-001 in Healthy

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

See also
Status	Clinical Trial	Phase
Completed	`NCT00765427` - Safety and Tolerability of Retinoid QLT091001 in Healthy Volunteers	Phase 1
Completed	`NCT04339283` - Effect of Standardized Hibiscus Sabdariffa Tea in Seemingly Healthy Human Volunteers	N/A
Completed	`NCT02219438` - Continuous Adductor Canal Nerve Blocks: Relative Effects of a Basal Infusion v. Hourly Bolus Doses	Phase 4

See also

Status

Clinical Trial

Phase

Completed

NCT00765427 - Safety and Tolerability of Retinoid QLT091001 in Healthy Volunteers

Phase 1

Completed

NCT04339283 - Effect of Standardized Hibiscus Sabdariffa Tea in Seemingly Healthy Human Volunteers

N/A

Completed

NCT02219438 - Continuous Adductor Canal Nerve Blocks: Relative Effects of a Basal Infusion v. Hourly Bolus Doses

Phase 4

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT00813670
Study type	Interventional
Source	Xenon Pharmaceuticals Inc.
Contact
Status	Completed
Phase	Phase 1
Start date	November 2008
Completion date	July 2009

Single and Multiple Ascending Dose Safety Study of XPF-001 in Healthy Volunteers

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms