Clinical Trial to Evaluate the Tolerability and Pharmacokinetics of a New Ultra Low Molecular Weight Heparin (RO-14) Administered Subcutaneously Increasing Single-doses to Healthy Male Volunteers
This study has been completed.
Sponsor:
Rovi Pharmaceuticals Laboratories
Information provided by:
Rovi Pharmaceuticals Laboratories
ClinicalTrials.gov Identifier:
NCT00629733
First received: February 15, 2008
Last updated: June 7, 2011
Last verified: June 2011
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Purpose
Clinical trial to evaluate the tolerability and pharmacokinetics of a new ultra low molecular weight heparin (RO-14) administered subcutaneously increasing single-doses to healthy male volunteers
| Condition | Intervention | Phase |
|---|---|---|
|
Healthy |
Drug: RO-14 |
Phase 1 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Pharmacokinetics Study Intervention Model: Crossover Assignment Masking: Open Label Primary Purpose: Treatment |
Resource links provided by NLM:
Further study details as provided by Rovi Pharmaceuticals Laboratories:
Primary Outcome Measures:
- Main objective : To evaluate safety and tolerability of increasing single-doses to healthy male volunteers [ Time Frame: safety parameters ] [ Designated as safety issue: Yes ]
Secondary Outcome Measures:
- Secondary objectives : To evaluate pharmacokinetics profiles of each of single-doses. [ Time Frame: anti-Xa activity ] [ Designated as safety issue: Yes ]
| Estimated Enrollment: | 12 |
| Study Start Date: | December 2007 |
| Study Completion Date: | December 2008 |
| Primary Completion Date: | December 2007 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Experimental: Ro-14 | Drug: RO-14 |
Eligibility| Ages Eligible for Study: | 18 Years to 45 Years |
| Genders Eligible for Study: | Male |
| Accepts Healthy Volunteers: | Yes |
Criteria
Inclusion Criteria:
- Healthy volunteers: male subjects aged between 18 and 45 years
- Body weight: 65-75 Kg
- Not meaningful abnormalities in physical examination and in clinical history
- Without evidence of significant organic or psychiatric illness
- Hemogram, biochemistry and coagulation in normal values established in the reference range of the local hospital laboratory
- Vital signs (blood pressure, heart beat rate and body temperature) and EKG within normal range
- Healthy volunteers who are not participating in another clinical trial or have not done so in the past 2 months
- Not give blood in the last 4 weeks.
- Healthy male volunteers who have not received heparin in the past
- Healthy male volunteers who have accepted to participate in the study and have signed the written informed consent
Exclusion Criteria:
- Previous history of alcoholism, drug dependency, drug abuse or habitual psychoactive drugs consumption
- Important consumption of exciting drinks: alcohol consumption > 30 g/day; coffee, tea, cola > 5 /day
- Allergy, idiosyncrasy or hypersensitivity to medicines
- Healthy volunteers who are receiving another medication in the past 15 days
- Positive serology of hepatitis B, C or HIV
- Cardiovascular, respiratory, renal, hepatic, endocrine, gastrointestinal, hematologic, psychiatric, neurological and others events
- Mayor Surgery in the last 6 months
- Smoking > 10 cigarettes / day
- Ethanol, cannabis, cocaine, amphetamine, benzodiazepine or opiate in urine
- Healthy volunteers with a familiar history evident hemorrhagic episodes
Contacts and Locations
More Information
No publications provided
| Responsible Party: | Dr. Barbanoj, Hospital Santa Creu i Sant Pau |
| ClinicalTrials.gov Identifier: | NCT00629733 History of Changes |
| Other Study ID Numbers: | ROV-RO14-2006-01 |
| Study First Received: | February 15, 2008 |
| Last Updated: | June 7, 2011 |
| Health Authority: | Spain: Spanish Agency of Medicines |
Keywords provided by Rovi Pharmaceuticals Laboratories:
|
pharmacokinetics ultra low molecular weight heparin |
Additional relevant MeSH terms:
|
Heparin, Low-Molecular-Weight Dalteparin Anticoagulants Hematologic Agents Therapeutic Uses |
Pharmacologic Actions Fibrinolytic Agents Fibrin Modulating Agents Molecular Mechanisms of Pharmacological Action Cardiovascular Agents |
ClinicalTrials.gov processed this record on June 18, 2013