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A Study to Evaluate Safety and Tolerability of BMN 111 Administered to Healthy Adult Volunteers

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.
ClinicalTrials.gov Identifier: NCT01590446
Recruitment Status : Completed
First Posted : May 3, 2012
Last Update Posted : June 11, 2012
Information provided by (Responsible Party):
BioMarin Pharmaceutical

Brief Summary:
The purpose of this study is to measure how much of the study drug gets into the blood- stream and how long it takes the body to get rid of it when given as a single dose. Information about any side effects that may occur will also be collected.

Condition or disease Intervention/treatment Phase
Achondroplasia Drug: BMN 111 Drug: Normal Saline Phase 1

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 74 participants
Allocation: Randomized
Intervention Model: Factorial Assignment
Masking: Double (Participant, Investigator)
Primary Purpose: Treatment
Official Title: A Phase 1, Two-Part, Double-Blind, Placebo-Controlled Study to Evaluate Safety, Tolerability, and Pharmacokinetics of Single and Multiple Doses of BMN 111 Administered to Healthy Adult Volunteers
Study Start Date : February 2012
Actual Primary Completion Date : June 2012
Actual Study Completion Date : June 2012

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Safety

Arm Intervention/treatment
Placebo Comparator: Placebo Drug: Normal Saline
SC injection, Part 1 single dose and Part 2 multiple dose

Active Comparator: BMN 111 Drug: BMN 111
SC injection, Part 1 single dose and Part 2 multiple dose.
Other Name: Modified C-Natriuretic Peptide, ProCNP38

Primary Outcome Measures :
  1. Safety based on vitals signs [ Time Frame: Daily throughout the study Assessed for approximately 8 days following each single dose in Part 1, and for approximately 24 days following each daily dose in Part 2 ]
  2. Safety based on adverse events [ Time Frame: Daily throughout the study Assessed for approximately 8 days following each single dose in Part 1, and for approximately 24 days following each daily dose in Part 2 ]

Secondary Outcome Measures :
  1. Pharmacokinetics [ Time Frame: Daily on dosing days Assessed during Part 1 for approximately 10 days and during Part 2 for approximately 24 days ]
  2. Safety based on cardiovascular effects [ Time Frame: Daily throughout the study Assessed for approximately 8 days following each single dose in Part 1, and for approximately 24 days following each daily dose in Part 2 ]

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

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Ages Eligible for Study:   22 Years to 45 Years   (Adult)
Sexes Eligible for Study:   Male
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • Is willing and able to provide written, signed informed consent (legally authorized representative) after the nature of the study has been explained and prior to performance of any research-related procedure.
  • Is a male 22 to 45 years of age, inclusive
  • Has a body weight between 63 and 100 kg, inclusive
  • Has a body mass index (BMI) between 18 and 32 kg/m2, inclusive
  • Is able and willing to abstain from nicotine, alcohol, methylxanthine-containing beverages or food (e.g., coffee, tea, colas, chocolate, energy drinks), poppy seeds, and grapefruit juice for 48 hours prior to admission and for the duration of the study
  • Is in good health generally, as determined by medical history, physical examination, clinical laboratory evaluations, and 12-lead electrocardiogram (ECG) at Screening
  • Is willing and able to perform all study procedures as physically possible
  • If sexually active, is willing to use a condom during sexual intercourse with female partners and to have their female partners use an additional effective means of contraception (e.g., intrauterine device, coil, diaphragm plus spermicide, oral contraceptive) or to abstain from sexual intercourse if female partner is not surgically sterile by tubal occlusion (ligation or occluding device) or postmenopausal from time of initial admission to the research facility until their last study visit

Exclusion Criteria:

  • Baseline systolic blood pressure < 100 mmHg
  • Subjects with spontaneous orthostatic hypotension, including a systolic decline of > 20 or diastolic change of > 10 mmHg or heart rate increase of > 30 bpm
  • Has renal insufficiency as determined by eGFR < 65 mL/min/1.73m2 using the revised Cockcroft-Gault calculation: (140 - age [y])
  • body weight [kg] / 72 serum creatinine [mg/dL]
  • Has anemia (Hb < 12.5 gm/dL)
  • Has history of cardiac or vascular disease, including the following: Congenital heart disease; Hypertension or hypotension; Cerebrovascular disease; aortic insufficiency; Clinically significant atrial or ventricular arrhythmias; Cardiac valvular heart disease; Hypertrophic cardiomyopathy or other cardiomyopathy
  • Has a Screening ECG showing any of the following: Resting heart rate < 45 or > 100 bpm; PR interval > 210 msec; P wave duration > 120 msec; QRS interval < 70 or > 120 msec; Corrected QTc > 440 msec; QRS axis outside the range of -30 + 100 degrees; Right or left atrial enlargement or ventricular hypertrophy; Second- or third-degree atrioventricular block
  • Heart block or intraventricular conduction defect
  • Has diabetes mellitus Type I or Type II
  • Is being treated with angiotensin-converting enzyme inhibitors, antihypertensive medications, diuretics, calcium-channel blockers, beta-blockers, cardiac glycosides, systemic anticholinergic agents, or drugs that may impair or enhance compensatory tachycardia
  • Is being treated with growth hormone, insulin-like growth factor 1 (IGF-1), or anabolic steroids.
  • Has any acute illness associated with volume dehydration (e.g., nausea/vomiting/diarrhea).
  • Uses of any prescription medications, over-the-counter medications, or nutritional supplements within 10 days prior to dosing.
  • Uses any other investigational product or investigational medical device within 90 days prior to screening or requires any investigational agent prior to completion of all scheduled study assessments.
  • Consumes at least 14 units/week of alcohol (1 unit approximates 360 mL beer, 100 mL wine, or 35 mL spirits) or has significant history of alcoholism or drug/chemical abuse as determined by the Investigator.
  • Has donated > 50 mL of blood or plasma within 60 days prior to study treatment administration.
  • Has a positive urine drug screen or alcohol breath test result during Screening or upon admission to the research facility.
  • Has used nicotine or tobacco-containing products (snuff, chewing tobacco, cigarettes,cigars, pipes, and nicotine replacements) within 90 days of the first dose of study treatment as confirmed by urine cotinine screen.
  • Has a positive cotinine test result during Screening or upon admission to the research facility.
  • Has a history of any clinically significant neurological, gastrointestinal, renal, hepatic, cardiovascular, psychiatric, respiratory, metabolic, endocrine, hematological, or other major disorders as determined by the Investigator.
  • Has had a clinically significant illness within 4 weeks of administration of the first dose of study treatment as determined by the Investigator.
  • Is being treated with a concomitant medication that prolongs the QT/QTc interval within 7 days or 3 half-lives, whichever is longer, prior to the Screening Visit.
  • Has AST or ALT greater than 3xULN or total bilirubin greater than 2xULN.
  • Has known hypersensitivity to BMN 111 or its excipients.
  • Has partner planning to become pregnant at any time during the study.
  • Has any condition that, in the view of the Investigator, places the subject at high risk of poor treatment compliance or of not completing the study.

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 ClinicalTrials.gov identifier (NCT number): NCT01590446

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United States, Indiana
Covance CRU Inc.
Evansville, Indiana, United States, 47710
Sponsors and Collaborators
BioMarin Pharmaceutical
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Responsible Party: BioMarin Pharmaceutical
ClinicalTrials.gov Identifier: NCT01590446    
Other Study ID Numbers: 111-101
First Posted: May 3, 2012    Key Record Dates
Last Update Posted: June 11, 2012
Last Verified: June 2012
Keywords provided by BioMarin Pharmaceutical:
Additional relevant MeSH terms:
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Bone Diseases, Developmental
Bone Diseases
Musculoskeletal Diseases
Genetic Diseases, Inborn