Trial | NCT00448071  Report issue

Title

Pharmacokinetic and Pharmacodynamic Effects of MTR107 in End-Stage Renal Disease (ESRD) Patients
A Phase II, Randomized Double Blind Placebo-Controlled, Dose Escalating Study to Determine Pharmacokinetic and Pharmacodynamic Effects of MTR107 in End-Stage Renal Disease (ESRD) Patients

  • Phase

    Phase 2

  • Study Type

    Interventional

  • Status

    Unknown status

  • Study Participants

    12
MTR107 effect on blood pressure throught the dialysis procedure and its ability to prevent Intra dialytic Hypotension
The present clinical trial aims to investigate and provide a more precise characterization of the pharmacokinetic and pharmacodynamic profile of MTR107 in a population of ESRD patients predisposed to developing intradialytic hypotension. The study is also designed as a dose esclating study aiming to assess MTR107 safety.
Study Started
May 31
2006
Study Completion
Mar 31
2007
Last Update
Mar 15
2007
Estimate

Drug MTR107

Criteria 

Inclusion Criteria:

Age 20-75 years, inclusive.
Presence of frequent bouts of hypotension defined as 3 or more intradialytic hypotensive events per month for the last six months prior to baseline, despite standard adjustments in dry weight.
ECG performed up to one month before study start.

Well-preserved hepatic function (within normal laboratory ranges) at study entry as judged by:

Serum Bilirubin (Total Bilirubin (direct and indirect) 0.3-1.0 mg/dL, and Direct Bilirubin 0.1-0.5 mg/dL)
Serum Albumin (>3.6 g/dL),
Serum aminotransferases (AST (0-37 U/L) and ALT (0-40 U/L)),
GGT (Gamma Glutamine Trans Peptidase)
Normal coagulation status at study entry as judged by PT-INR, PTT, fibrinogen and platelet count.
Willingness to participate in the study and adhere to the study design.
Willingness to sign an informed consent form.

Exclusion Criteria:

Uncontrolled hypertension >140/90 mmHg.
Unstable angina.
Abnormal ECG which may indicate acute disease
Variable weight gains.
Mental retardation.
Pregnancy.
Malignancy or other concomitant serious diseases.
Current participation in another clinical trial involving an investigational drug/device, or participation in such a trial within the last 30 days.
No Results Posted