An Exploratory Study to Evaluate FMX-8 to Treat Anemia in CKD

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Pharmacodynamics Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

See also
Status	Clinical Trial	Phase
Completed	`NCT01978587` - Effect of Hemodialysis on the PK of JTZ-951 in Subjects With End-stage Renal Disease	Phase 1
Completed	`NCT04197778` - Food Effect Study of DDO-3055 Tablets in Healthy Subjects	Phase 1
Completed	`NCT01599507` - Study of FG-4592 in Subjects With Chronic Kidney Disease in China	Phase 2

See also

Status

Clinical Trial

Phase

Completed

NCT01978587 - Effect of Hemodialysis on the PK of JTZ-951 in Subjects With End-stage Renal Disease

Phase 1

Completed

NCT04197778 - Food Effect Study of DDO-3055 Tablets in Healthy Subjects

Phase 1

Completed

NCT01599507 - Study of FG-4592 in Subjects With Chronic Kidney Disease in China

Phase 2

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	NCT02228655
Study type	Interventional
Source	FerruMax Pharmaceuticals, Inc.
Contact
Status	Terminated
Phase	Phase 0
Start date	October 2014
Completion date	July 2015

An Exploratory Study to Evaluate FMX-8 to Treat Anemia in CKD

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms