The Safety, Tolerability And Metabolism Of GSK221149A, In Pregnant Women (30-36 Weeks), In Pre-Term Labor



Status:Completed
Conditions:Women's Studies
Therapuetic Areas:Reproductive
Healthy:No
Age Range:18 - 45
Updated:1/17/2018
Start Date:October 12, 2007
End Date:July 7, 2011

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A Randomized, Double-blind, Placebo-controlled, Dose Ranging Study to Investigate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of GSK221149A Administered Intravenously and to Investigate the Pharmacokinetics of GSK221149A Administered Orally to Healthy, Pregnant Females With Uncomplicated Pre-term Labor Between 300/7 and 356/7 Weeks' Gestation

Pre-Term Labor (prior to 37 weeks gestation) is the largest single cause of infant morbidity
and mortality and is frequently associated with long-term disability. Oxytocin is a hormone
produced by the body during labor. GSK221149A is an experimental drug that will be used to
block the effects of oxytocin, and therefore pause or prevent contractions. In this study,
patients with preterm labor will be given an intravenous infusion of GSK221149A over
approximately 12 hours followed by an oral tablet in Parts A and B. In part C of this study,
patients with preterm labor will be give an intravenous infusion of GSK221149A over
approximately 48 hours. The use of a rescue tocolytic is allowed in the study.

A randomized, double-blind, placebo-controlled, dose ranging study to investigate the safety,
tolerability, pharmacokinetics and pharmacodynamics of GSK221149A administered intravenously
and to investigate the pharmacokinetics of GSK221149A administered orally to healthy,
pregnant females with uncomplicated pre-term labor between 300/7 and 356/7 weeks' gestation

Inclusion criteria:

- Healthy pregnant females, 30 -36 weeks pregnant, without ruptured membranes

- 18-45 inclusive

- Symptoms of pre-term labor, (greater than or equal to 6 uterine contractions per hour,
each of which at least 30 sec in duration, with cervical dilatation of less than or
equal to 4 cm, (measured by tocodynamometry).

Exclusion criteria:

- Any clinically relevant abnormality identified on the screening examination or any
other medical condition or circumstance making the patient (mother and/or fetus)
unsuitable for participation in the study

- Any clinically relevant pre-existing or pregnancy-related co-morbid condition that may
affect maternal pregnancy outcome or neonatal outcome (eg. hypertension, diabetes
mellitus, bleeding/clotting diathesis)
We found this trial at
30
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Southern Pines, North Carolina 28388
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Chapel Hill, North Carolina 27599
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Charleston, South Carolina 29425
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Chattanooga, Tennessee 37421
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Cincinnati, Ohio 45229
727
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Ciudad Autonoma de Buenos Aires, Buenos Aires
5602
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Ciudad Autonoma de Buenos Aires,
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Colton, California 92324
1117
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Columbia, South Carolina 29203
969
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Galveston, Texas 77555
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Houston, Texas 77030
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Idaho Falls, Idaho 83404
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Jonesboro, Arkansas 72401
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Kansas City, Kansas 66160
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Knoxville, Tennessee 37916
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Loma Linda, California 92357
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Los Angeles, California 90025
1179
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Memphis, Tennessee 38120
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Minneapolis, Minnesota 55404
551
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Mobile, Alabama 36617
737
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Mobile, AL
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New York, New York 10032
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Newark, Delaware 19713
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Newark, New Jersey 07112
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Norfolk, Virginia 23502
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Philadelphia, Pennsylvania 19104
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Phoenix, Arizona 85012
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Saint Louis, Missouri 63110
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Salt Lake City, Utah 84132
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Tucson, Arizona 85724
833
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West Jordan, Utah 84088
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Winston-Salem, North Carolina 27103
971
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Winston-Salem, NC
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