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HealthyPhase 1NCT00618579

Effects of LMWH in Healthy Subjects Treated With TB-402 and Effects of TB-402 in Healthy Subjects Treated With Warfarin

A Phase 1 study testing LWMH in TB-402 treated subjects or TB-402 in warfarin treated subjects in people with Healthy, run by ThromboGenics at 1 site in Denmark.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Administration of LMWH in healthy male subjects treated with TB-402 and administration of TB-402 in healthy male subjects treated with warfarin Read more about this study

Who is it for?
Ages 18 to 45 years, men onlyHealthy volunteers can take part
Conditions the study is for
Healthy
What is being tested?
LWMH in TB-402 treated subjects or TB-402 in warfarin treated subjects
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
15 participants
Where
1 siteDenmark
Study dates
Feb 2008to Aug 2008
Phase
Phase 1
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 45 years
  • Men only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Males 18 to 45 years of age
  • Healthy according to medical history, physical exam, ECG, blood pressure and heart rate, and laboratory profile of blood and urine

Who cannot join

  • Self or family history of cardiovascular or pulmonary disorder, or coagulation or bleeding disorders or reasonable suspicion of vascular malformations e.g. cerebral haemorrhage, aneurysm or premature stroke
  • History of important bleeding episodes
  • Previous allergic reaction to immunoglobulin
  • Present or previous history of severe allergy, for example asthma or anaphylactic reactions
  • FVIII:C <50% at screening
  • Clinically significant out of range values for any coagulation test during screening
  • Received prescribed medication, over the counter medication or herbal medicines within 14 days of receipt of TB-402

Trial locations and contacts

1 site in 1 country.

Denmark1 site
  • Cyncron CRU

    Copenhagen

Other trials in Denmark

About this study

Official title: A Randomised, Controlled Study Investigating the Safety and Anticoagulant Activity of Administration of Low-molecular-weight Heparin in Healthy Male Subjects Treated With the Monoclonal Anti-factor VIII Antibody, TB-402 and the Safety and Anticoagulant Activity of Administration of TB-402 in Healthy Male Subjects Treated With Warfarin

Administration of LMWH in healthy male subjects treated with TB-402 and administration of TB-402 in healthy male subjects treated with warfarin

Conditions
Healthy
Being tested
LWMH in TB-402 treated subjects or TB-402 in warfarin treated subjects
Keywords
Interaction with LMWH or warfarin

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • LWMH in TB-402 treated subjects or TB-402 in warfarin treated subjectsDrug

    Administration of LMWH in healthy male subjects treated with TB-402 and administration of TB-402 in healthy male subjects treated with warfarin

Study groups in NCT00618579
Study groupRoleWhat they receive
LMWH arm - active LMWHExperimentalNot described
Receives: Drug: LWMH in TB-402 treated subjects or TB-402 in warfarin treated subjects
LMWH arm - placeboPlacebo comparatorNot described
Receives: Drug: LWMH in TB-402 treated subjects or TB-402 in warfarin treated subjects
Warfarin arm - active warfarinExperimentalNot described
Receives: Drug: LWMH in TB-402 treated subjects or TB-402 in warfarin treated subjects
Warfarin arm - controlOtherNot described
Receives: Drug: LWMH in TB-402 treated subjects or TB-402 in warfarin treated subjects

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Anticoagulant activity assessed by aPTT, PT, TGAs and FVIII:c

    Measured: To study end

Secondary outcomes (1)
  1. Changes in safety parameters over time, PK parameters estimated by NCA, effect of LMWH in TB-402 treated subjects assessed by anti factor Xa (LMWH arm)

    Measured: To study end

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Feb 2008 (estimated)
  2. Study startFeb 2008
  3. Primary completionJun 2008
  4. Study completionAug 2008

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
15 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00618579
Sponsor's protocol ID
TB-402-003
Status last verified
Apr 2014
First submitted
28 Jan 2008
Last updated
7 Apr 2014
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A Phase 1 study testing LWMH in TB-402 treated subjects or TB-402 in warfarin treated subjects in people with Healthy, run by ThromboGenics at 1 site in Denmark.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 7 Apr 2014. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Denmark. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Anticoagulant activity assessed by aPTT, PT, TGAs and FVIII:c (time frame: To study end). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 Apr 2014.

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