ProHealth health Vitamin and Natural Supplement Store and Health
Home  |  Log In  |  My Account  |  View Cart  View Your ProHealth Vitamin and Supplement Shopping Cart
800-366-6056  |  Contact Us  |  Help
Facebook Google Plus
Fibromyalgia  Chronic Fatigue Syndrome & M.E.  Lyme Disease  Natural Wellness  Supplement News  Forums  Our Story
Store     Brands   |   A-Z Index   |   Best Sellers   |   New Products   |   Deals & Specials   |   Under $10   |   SmartSavings Club

Trending News

Curcumin: The All In One Solution, Part 2

CoQ10 — A Nutritional Powerhouse for Mitochondrial Health

How to Prevent Hearing Loss and Improve Your Hearing With Nutrition

What Are the Benefits of Vitamin K2?

Vitamin D deficiency + high fat diet = metabolic syndrome

Use Burdock Oil to Promote Healthy Hair Growth

Why You Should Take Your Apple Cider Vinegar at Night

AMA journal associates iron deficiency with hearing loss

Lutein linked to preservation of crystallized intelligence

Zinc eaten at levels found in biofortified crops reduces 'wear and tear' on DNA

Print Page
Email Article

Efficacy and Safety of Oral Growth Hormone Stimulating Drug in Treatment of Fibromyalgia

  [ 489 votes ]   [ Discuss This Article ]
By Editor • • February 2, 2007

A 24-week Phase II trial - directed by FM specialist Robert Bennett, MD, at Oregon Health & Science University in Portland, and sponsored by Merck - is recruiting female FM patients between the ages of 30 and 65.

The study is a randomized, double-blind, placebo-controlled trial to evaluate the safety, tolerability and efficacy of an orally administered growth hormone stimulating drug (code named MK-0677) in the treatment of female subjects with primary Fibromyalgia.

“The rationale for this study is the observation that many Fibromyalgia patients are growth hormone deficient in terms of low levels of IGF-1, and that improving IGF-1 levels with growth hormone injections has been shown to improve Fibromyalgia symptoms.” That is, it follows a trial of growth hormone injections for Fibromyalgia patients that “produced promising results, with significant improvements in physical functioning (FIQ), number of tender points, and global improvement, compared to the placebo group.”

The official name of the trial is “Efficacy and Safety of an Oral Growth Hormone Drug in the Treatment of Fibromyalgia” ( number NCT00116129).

Primary Outcomes Measured
n Is MK-0677 25 mg superior to placebo in reducing symptoms of Fibromyalgia, as assessed by the Fibromyalgia Impact Questionnaire (FIQ) over a 24-week treatment period?
n Is MK-0677 25 mg generally safe and well tolerated in subjects with Fibromyalgia?

Secondary Outcomes Measured
n Is MK-0677 25 mg superior to placebo in reducing muscle tenderness, as assessed by the Fibromyalgia Myalgic Score (FMyS)?
n Is MK-0677 25 mg superior to placebo in improving the subjects’ global perception of change in Fibromyalgia symptoms, as assessed by the Subjects' Global Impression of Change Questionnaire (PGIC)?
n Is MK-0677 25 mg is superior to placebo in improving the subjects’ quality of life, as assessed by the Quality of Life Questionnaire (QOL)?

About the Drug
“MK-0677 is an orally administered growth hormone secretagogue manufactured by Merck & Co., Inc. that acts on the growth hormone secretagogue receptor in the anterior pituitary to stimulate the release of growth hormone. This pathway represents an additional regulation of growth hormone release from pituitary somatotrophs to that mediated by growth hormone releasing hormone (stimulating) and somatostatin (inhibitory).

“Both stimulatory pathways lead to a pulsatile release of growth hormone, with approximately 4 hour intervals between peak levels. This growth hormone secretion leads to a rapid and robust up regulation of IGF-1 levels by about 50 to 100% that can be maintained with chronic therapy at a dose of 25 mg/day.”

Requirements for Inclusion:
n Subjects will all be female primary fibromyalgia subjects who are 30 to 65 years of age, inclusive, and have a low age adjusted serum IGF-1 level.
n All subjects will fulfill a diagnosis of fibromyalgia according to the classification criteria of the American College of Rheumatology (ACR).
n All subjects will have an initial Fibromyalgia Impact Questionnaire (FIQ) score = 40. n If subject is of childbearing potential and sexually active, she agrees to use effective barrier or appropriate oral contraception during the study. Subjects who are taking oral contraceptives must have done so for at least 2 months prior to entering the study.
n Subject is not pregnant and is not nursing.
n Patient has a normal screening breast exam. If screening breast exam is abnormal, but not suggestive of breast cancer, the patient must have had a normal mammogram within the last 6 months.
n Subject has a normal screening stool hemoccult. If the screening stool hemoccult is abnormal, but likely due to hemorrhoids, the subject must have had a normal sigmoidoscopy within the last 2 years.
n Subject is willing to discontinue using grapefruit juice for duration of study.
n Subject is willing to be followed by telephone contact for 3 months after she has discontinued study and completed and returned the Fibromyalgia Impact Questionnaire, Patient Global Change score, Quality of Life score, Brief Pain Inventory and Beck Depression Questionnaire.

Exclusion Criteria:
n Subject has an-ongoing, unresolved disability litigation.
n Subject has diabetes or a significantly elevated random glucose at the Screening visit.
n Subject has a current or past history of cardiovascular, pulmonary, neurological, endocrine or renal disease that would preclude involvement in an exercise program (specifically hypertension, a myocardial infarction within the last 6 months, chronic obstructive pulmonary disease [COPD], asthma, untreated hypothyroidism, severe depression with suicide risk, previous pituitary disease or surgery).
n Subject has a history of angina or congestive heart failure with symptoms that occur at rest.
n Subject has a history or current evidence of a psychotic disorder (e.g. schizophrenia), bipolar disorder or major depression, or substance abuse by DSM-IV criteria; severe depression, as evidenced by a Beck Depression score of = 30.
n Subject has history of neurological disorder other than Fibromyalgia (e.g. epilepsy, stroke, neuropathy, neuropathic pain).
n Subject has ongoing symptoms of carpal tunnel syndrome.
n Subject has any other significant pain state, i.e. subject must have primary Fibromyalgia.
n Subject has a history of hepatitis or liver disease that has been active within the past 12 weeks.
n Subject has cancer or a history of cancer within the past 2 years, or a history of cancer of more than 2 years ago and deemed to not be cured, or subject has ANY history of breast cancer. (NOTE: Subjects with a history of basal cell or squamous cell carcinoma of the skin treated more than 1 year ago and with no evidence of recurrence may participate.)
n Subject has abnormal thyroid stimulating-hormone, or T4 concentrations.
n Subject has a planned elective surgery during the study period.
n Subject has a history of hypersensitivity or idiosyncratic
reaction to more than 2 drug classes (by chemical classification).
n Subject has abnormal Screening visit laboratory values.
n Subject is using any of the following medications : heparin, ticlopidine, ginko (in subjects taking warfarin), oral steroids (>/= 7 days per month), chronic use of strong CYP3A4 inhibitors (HIV protease inhibitors, macrolide antibiotics and nefazodone), chronic use of CYP3A4 inducers (carbamazepine, phenytoin, rifampin, and St. John’s Wort).
n Subject has received an investigational drug or device within 30 days of study entry.

Location and Contact Information
Please refer to this study by identifier NCT00116129
Oregon Health & Science University, Portland

Principal Investigator Robert Bennett, MD 503-494-1793

Sub-Investigator Kim Jones, FNP, PhD 503-494-3837

Health Authority: US Food and Drug Administration

Post a Comment

Featured Products From the ProHealth Store
Optimized Curcumin Longvida® Ultra EPA  - Fish Oil Ultra ATP+, Double Strength

Looking for Vitamins, Herbs and Supplements?
Search the ProHealth Store for Hundreds of Natural Health Products

Article Comments

Be the first to comment on this article!

Post a Comment

NAD+ Ignite with Niagen

Featured Products

Ultra EPA  - Fish Oil Ultra EPA - Fish Oil
Ultra concentrated source of essential fish oils
Mitochondria Ignite™ with NT Factor® Mitochondria Ignite™ with NT Factor®
Reduce Fatigue up to 45%
Ultra ATP+, Double Strength Ultra ATP+, Double Strength
Get energized with malic acid & magnesium
Vitamin D3 Extreme™ Vitamin D3 Extreme™
50,000 IU Vitamin D3 - Prescription Strength
Energy NADH™ 12.5mg Energy NADH™ 12.5mg
Improve Energy & Cognitive Function

Natural Remedies

More Weight Loss than Any Other Discovery in Supplement History More Weight Loss than Any Other Discovery in Supplement History
Itching to Find Dry Skin Relief? Itching to Find Dry Skin Relief?
Irritable Bowel Syndrome: Unlocking the Secrets of Peppermint, Acacia and Fennel Irritable Bowel Syndrome: Unlocking the Secrets of Peppermint, Acacia and Fennel
Natural Support for Mood, Sleep and Mental Focus? L-theanine Natural Support for Mood, Sleep and Mental Focus? L-theanine
Why Berries Offer a Rainbow of Health Benefits Why Berries Offer a Rainbow of Health Benefits

ProHealth, Inc.
555 Maple Ave
Carpinteria, CA 93013
(800) 366-6056  |  Email

· Become a Wholesaler
· Vendor Inquiries
· Affiliate Program
Credit Card Processing
Get the latest news about Fibromyalgia, M.E/Chronic Fatigue Syndrome, Lyme Disease and Natural Wellness

CONNECT WITH US ProHealth on Facebook  ProHealth on Twitter  ProHealth on Pinterest  ProHealth on Google Plus

© 2017 ProHealth, Inc. All rights reserved. Pain Tracker App  |  Store  |  Customer Service  |  Guarantee  |  Privacy  |  Contact Us  |  Library  |  RSS  |  Site Map