A Study of SB751689 in Japanese Postmenopausal Women

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00554255
Recruitment Status : Completed
First Posted : November 6, 2007
Last Update Posted : August 29, 2018
Information provided by (Responsible Party):

Brief Summary:
To investigate the safety and tolerability, PK and PD of SB751689 following single and 5-day multiple oral doses of 100, 200, and 400 mg in Japanese postmenopausal subjects.

Condition or disease Intervention/treatment Phase
Osteoporosis Drug: SB751689 Phase 1

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 18 participants
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Single (Participant)
Primary Purpose: Treatment
Official Title: Phase I Study of SB751689 - Single and Multiple Oral Dose Study in Japanese Postmenopausal Women -
Study Start Date : October 23, 2006
Actual Study Completion Date : December 12, 2006

Primary Outcome Measures :
  1. Adverse events, change in clinical laboratory tests, vital signs, 12lead ECG [ Time Frame: throughout the study ]

Secondary Outcome Measures :
  1. Pharmacokinetics and Pharmacodynamics of SB751689 [ Time Frame: throughout the study ]

Information from the National Library of Medicine

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Ages Eligible for Study:   50 Years to 70 Years   (Adult, Older Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • The subject is considered as healthy by the investigator at screening.
  • Healthy subjects are defined as individuals who are free from clinically significant illness or disease as determined by their medical history, physical examination, laboratory studies, and other tests
  • Japanese healthy postmenopausal woman as defined as being amenorrheic for at least 1 year at screening with <157.79mIU/mL of FSH levels.
  • Body weight >= 45 kg and BMI within the range 18.5 -25.0 kg/m2.
  • The subject is within the following criteria as screening;Liver function tests (ALT, AST, GGT, alkaline phosphatase, total bilirubin), CPK, serum parathyroid hormone (iPTH) test, vitamin D (1,25(OH2 D3)) levels, Serum calcium
  • Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.
  • Non-smokers (at least 6 months)
  • The subject is able to attend all visits and complete the study.

Exclusion Criteria:

  • The subject has any clinically relevant abnormality on medical examination, vital sign, clinical laboratory test or medical history at screening in the medical opinion of the investigator or the subject has a medical history that is not considered as eligible for inclusion in this study by the investigator.
  • History of sensitivity to any of the study medications or components thereof (except pollenosis without any signs or symptoms).
  • Participation in a clinical study or post-marketing study with an investigational or a non-investigational product or device within 4 months of preceding the first dose of study medication.
  • Participation in another clinical study or post-marketing study in which the subject is or will be exposed to an investigational or a non-investigational product or device.
  • Positive for syphilis, HIV antibody, hepatitis B antigen or hepatitis C antibody, HTLV-1 antibody at screening.
  • Positive urine drug screen at screening.
  • Donation of blood in excess of 400 mL within the previous 4 months or 200mL within the previous 1 month of screening.
  • Use of prescription or non-prescription drugs, herbal and dietary supplements, within 14 days prior to the first dose of study medication.
  • History of drug abuse or current conditions of drug abuse or alcoholism.
  • History of regular alcohol consumption exceeding 7 units/week (>350mL of beer/unit) within 6 months of screening.
  • Subjects with a history of renal, hepatic, or biliary disease.
  • History of clinically significant cardiovascular disease.
  • History of pernicious anemia, pancreatitis, osteosarcoma or kidney stones.
  • Subjects who have had history of significant gastrointestinal disease (e.g., gastrointestinal malabsorptive disease, colostomy, chronic gastroesophageal reflux disease, Crohn's disease, ulcerative colitis, gastric or duodenal ulcer, gastrointestinal tract bleeding, short bowel syndrome, sprue, lactose intolerance, irritable bowel syndrome).
  • Subjects with any history of a gastrointestinal surgical procedure that might affect the absorption of SB-751689 (e.g. cholecystectomy, gastrointestinal bypass surgery, partial or total gastrectomy, small bowel resection).
  • Medical conditions which might alter bone metabolism, including hyperparathyroidism, hypoparathyroidism, hyperthyroidism, hypothyroidism, Paget's disease, malabsorption, or Cushing's syndrome, and hypogonadism, hypocalcemia, hypercalcemia, hypophosphatemia, hypomagnesemia, hypermagnesemia, osteopetrosis, osteomalacia, and recent (within one year) history of fracture or prolonged bedrest.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00554255

Sponsors and Collaborators
Study Director: GSK Clinical Trials GlaxoSmithKline

Responsible Party: GlaxoSmithKline Identifier: NCT00554255     History of Changes
Other Study ID Numbers: 108543
First Posted: November 6, 2007    Key Record Dates
Last Update Posted: August 29, 2018
Last Verified: August 2018

Keywords provided by GlaxoSmithKline:

Additional relevant MeSH terms:
Bone Diseases, Metabolic
Bone Diseases
Musculoskeletal Diseases
Metabolic Diseases