FDA Halts Study on Dietary Supplements
Posted on: Wednesday, 9 April 2003, 06:00 CDT
Naval Academy study ends prematurely
ANNAPOLIS, Md. (AP) -- The Food and Drug Administration halted a study of the effects of dietary supplements on Naval Academy midshipmen because of concerns about privacy, record-keeping and other issues.
The FDA said researchers couldn't account for the medical records of at least 92 of the 260 midshipmen, and FDA Commissioner Mark B. McClellan asked for an investigation by Janet Rehnquist, the Department of Health and Human Services' inspector general.
"As the institution of the federal government that oversees the integrity of much of the nation's clinical trials, I want to assure that FDA is held to the same - if not higher - standards regarding clinical trial conduct to which we hold others," McClellan said in a letter obtained by The (Baltimore) Sun.
McClellan also ordered the FDA's six research centers to review procedures and policies for monitoring agency-sponsored clinical studies, the newspaper reported Wednesday.
FDA officials said there is no evidence showing midshipmen were harmed or that their records wound up in the wrong hands.
The clinical trial, led by FDA calcium expert Dr. Mona S. Calvo, examined whether midshipmen who ate specially formulated nutrition bars developed denser bones.
Paid for by a $610,000 grant from the Army, the study is part of an effort to determine the best mix of dietary calcium, protein, potassium and vitamin K to help reduce bone fractures suffered by troops during training.
About 260 midshipmen from the class of 2003 were recruited in 1999 for the study. The students agreed to provide blood and urine samples, undergo bone scans and share dietary records.
Within a year, the number of participants was down to 52, so few that Calvo was no longer able to collect statistically significant data, according to FDA documents.
The FDA began reviewing the study following an exchange of charges between Calvo and fellow researcher, Dr. David W. Armstrong III of the Henry M. Jackson Foundation for the Advancement of Military Medicine, a private group in Rockville.
A telephone call by The Associated Press to Calvo's office, seeking comment from the researcher, was not immediately returned Wednesday.
Other problems noted by the FDA included alleged failure to perform some pregnancy screenings and inability to account for the nutritional bars.
---
On the Net:
U.S. Food and Drug Administration
More science, space, and technology from RedNova
Copyright © 2003 The Associated Press. All rights reserved. The information contained in the AP News report may not be published, broadcast, rewritten or redistributed without the prior written authority of The Associated Press.
Related Articles
- FDA Study Indicates Most Industry Postmarketing Studies Meet Timelines
- ATS Medical Announces FDA Approval for a Landmark Clinical Investigation of the ATS 3f Aortic Bioprosthesis
- Electronic Cigarette Company (eCigarettesChoice.com) Claims FDA Study Proves E-Cigarettes Are Safer Than Tobacco Cigarettes
- FDA Study Links Insulin Pumps to Teenage Injuries, Deaths
- Netsmart Technologies Announces Development Program on Microsoft for Local Public Health Clinic Management and Vital Records Software
- Capital Orthopaedic &Amp; Sports Medicine Center Deploys SRSsoft Clinical Manager(TM) in a Record 44 Business Days
- Hollis-Eden Pharmaceuticals Cleared By FDA to Initiate Phase I Clinical Trial With HE3286 in Treating Metabolic Disorders
- FermaVir Announces FDA Response to Its Pre-IND Submission for Initial Bioavailability Studies in Human Clinical Trials of FV-100; Response Enables Company to Plan Clinical Development Program for Novel Antiviral Drug Candidate
- Under Amendment, FDA Could Require Additional Clinical Trials of Drugs
- Spine Wave Notifies Protein Polymer Technologies of FDA Approval to Conduct U.S. Clinical Trials
User Comments (0)


RSS Feeds