Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2015:116:19-27.
doi: 10.1093/bmb/ldv045. Epub 2015 Nov 17.

Human embryonic and induced pluripotent stem cells in clinical trials

Affiliations
Review

Human embryonic and induced pluripotent stem cells in clinical trials

Dusko Ilic et al. Br Med Bull. 2015.

Abstract

Background: Human embryonic and induced pluripotent stem cells (hESC and hiPSC) have tremendous potential for clinical implementation. In spite of all hurdles and controversy, clinical trials in treatment of spinal cord injury, macular degeneration of retina, type 1 diabetes and heart failure are already ongoing.

Sources of data: ClinicalTrials.gov database, International Clinical Trials Registry Platform, PubMed and press releases and websites of companies and institutions working on hESC- and iPSC-based cellular therapy.

Areas of agreement: The initial results from multiple clinical trials demonstrate that hESC-based therapies are safe and promising.

Areas of controversy: Are iPSC cells safe in the clinical application? Is there a room for both hESC and iPSC in the future clinical applications?

Growing points: Increasing number of new clinical trials.

Areas timely for developing research: Development of hESC- and/or iPSC-based cellular therapy for other diseases.

Keywords: diabetes; heart repair; human embryonic stem cells (hESC); human induced pluripotent stem cells (hiPSC); macular degeneration; spinal cord injury.

PubMed Disclaimer

MeSH terms