Other Clinical Trial - Safety & Efficacy of CKDB-501A in Subjects With

See also
Status	Clinical Trial	Phase
Active, not recruiting	`NCT05940805` - Comprehensive Protocol for Treatment of Upper Limb Spasticity in Post-stroke Hemiplegic Patients	N/A
Completed	`NCT00432666` - IncobotulinumtoxinA (Xeomin) Versus Placebo in the Treatment of Post-stroke Spasticity of the Upper Limb	Phase 3
Completed	`NCT03131791` - Comparing the Radial Extracorporeal Shock Waves and Botulinum Toxin Injection for Spasticity	N/A

See also

Status

Clinical Trial

Phase

Active, not recruiting

NCT05940805 - Comprehensive Protocol for Treatment of Upper Limb Spasticity in Post-stroke Hemiplegic Patients

N/A

Completed

NCT00432666 - IncobotulinumtoxinA (Xeomin) Versus Placebo in the Treatment of Post-stroke Spasticity of the Upper Limb

Phase 3

Completed

NCT03131791 - Comparing the Radial Extracorporeal Shock Waves and Botulinum Toxin Injection for Spasticity

N/A

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	NCT05382767
Study type	Interventional
Source	CKD Bio Corporation
Contact
Status	Completed
Phase	Phase 1
Start date	June 2, 2022
Completion date	December 8, 2022

Safety and Efficacy of CKDB-501A in Subjects With Post-stroke Upper Limb Spasticity

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms