Study Of Single Ascending Doses Of PBL 1427 In Healthy Volunteers

This study is currently recruiting participants.
Verified May 2013 by Panacea Biotec Ltd
Sponsor:
Information provided by (Responsible Party):
Panacea Biotec Ltd
ClinicalTrials.gov Identifier:
NCT01554293
First received: February 17, 2012
Last updated: May 15, 2013
Last verified: May 2013

February 17, 2012
May 15, 2013
July 2012
July 2013   (final data collection date for primary outcome measure)
  • Number of subjects with adverse events [ Time Frame: Pre-dose and upto Day 5-9 ] [ Designated as safety issue: Yes ]
    Safety and tolerability of PBL 1427 will be assessed after single ascending doses when administered alone on the basis of AEs, vital signs (BP, pulse rate, and body temperature), ECG, laboratory parameters and clinical assessment.
  • Pharmacokinetics Variables (Cmax, tmax, AUC, t1/2, kel, CL/F & Vz/F) [ Time Frame: 48 hrs post dose ] [ Designated as safety issue: No ]
    Pharmacokinetic parameters of single ascending doses of PBL 1427 : For each subject, blood will be collected at the following time points: pre-dose, 0.25, 0.50, 0.75 1, 1.5, 2, 3, 4, 6, 8, 10, 14, 16, 20, 24, 36 and 48 h post-dose.
Same as current
Complete list of historical versions of study NCT01554293 on ClinicalTrials.gov Archive Site
  • Pharmacodynamics assessment (glucose, insulin, C-peptide, lactic acid) [ Time Frame: Pre-dose and upto 4 h post-dose ] [ Designated as safety issue: No ]
    Pharmacodynamics will be assessed using markers like glucose, insulin, C-peptide, lactic acid and the exploratory markers plasma DPP-IV activity and plasma GLP-1 (Glucagon-like peptide I) levels
  • Exploratory markers (plasma DPP-IV activity and GLP-1 levels) [ Time Frame: Pre-dose and upto 48 h after dosing ] [ Designated as safety issue: No ]
    Pharmacodynamics will be assessed using markers like glucose, insulin, C-peptide, lactic acid and the exploratory markers plasma DPP-IV activity and plasma GLP-1 (Glucagon-like peptide I) levels
Same as current
Not Provided
Not Provided
 
Study Of Single Ascending Doses Of PBL 1427 In Healthy Volunteers
A Randomized, Double-Blind, Placebo-Controlled Phase I Study To Determine The Safety, Tolerability, Pharmacokinetics And Pharmacodynamics Of Single Ascending Doses Of PBL 1427 In Healthy Volunteers

PBL 1427 is a Dipeptidyl peptidase (DPP)-IV inhibitor being developed for treatment of type 2 diabetes. Although a number of DPP-IV inhibitors have been described, there still exists a need for new DPP-IV inhibitors that have better half-life, advantageous potency, stability and selectivity, less toxicity and/or better pharmacodynamic properties.

As per the randomization schedule, capsule(s) of A or B will be administered to each subject with 240 mL of water at ambient temperature. Subjects will be instructed not to chew or crush the capsule(s) but to consume it as a whole. Compliance for dosing will be assessed by a thorough check of the oral cavity immediately after dosing. Administration of investigational products will be carried out while the subjects are in sitting posture and they will be instructed to remain seated for two hours after dosing except when clinically indicated to change the posture or in case of any natural exigency. Thereafter, the subjects will be allowed to engage in normal activities while avoiding severe physical exertion.

The following treatments in the below cohorts will be followed as given below:

Cohort 1: A single oral dose of 20 mg of PBL 1427 (n=6) or placebo (n=2) Cohort 2: A single oral dose of 40 mg (20 mg X 2 capsules) of PBL 1427 (n=6) or placebo (n=2) Cohort 3: A single oral dose of 80 mg (20 mg X 4 capsules) of PBL 1427 (n=6) or placebo (n=2) Cohort 4: A single oral dose of 150 mg of PBL 1427 (n=6) or placebo (n=2) Cohort 5: A single oral dose of 300 mg (150 mg X 2 capsules) of PBL 1427 (n=6) or placebo (n=2) Cohort 6: A single oral dose of 600 mg (150 mg X 4 capsules) of PBL 1427 (n=6) or placebo (n=2)

Dose levels may be modified and intermediate dose levels might be tested to determine the maximum tolerated dose (MTD)

The number of cohorts, dose levels, frequency and conditions of administration for the subsequent cohort may be altered by the Principal investigator and Sponsor after evaluation of the results of the previous group.

Interventional
Phase 1
Allocation: Randomized
Endpoint Classification: Pharmacokinetics/Dynamics Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Diabetes Mellitus
  • Drug: Matching placebo
    Matching Placebo, single dose
  • Drug: PBL 1427 capsules
    PBL 1427 capsules 20 mg and 150 mg, single dose
  • Experimental: PBL 1427 capsules
    Intervention: Drug: PBL 1427 capsules
  • Placebo Comparator: Matching placebo
    Intervention: Drug: Matching placebo
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
48
September 2013
July 2013   (final data collection date for primary outcome measure)

Inclusion Criteria: Subjects to be enrolled in this trial must fulfil all of these criteria:

  • Sex: male
  • Age: 18-60 yr old, both inclusive
  • Having a Body Mass Index (BMI) between 18.5-28 kg / m2 (both inclusive) and body weight not less than 45 kg
  • Full comprehension: ability to comprehend the full nature and purpose of the study, including possible risks and side effects; and to comply with the requirements of the entire study
  • Voluntarily given written informed consent to participate in this study
  • Be of normal health as determined by the principal investigator from medical history, physical examination and laboratory investigations, 12- lead ECG and X-ray chest of the subjects performed within 10 days prior to the admission of the study
  • Ability and willingness to abstain from alcohol, methylxanthine-containing beverages or food (coffee, tea, coke, chocolate, "power drinks") and grapefruit (juice) from 48 h prior to each admission until study completion

Exclusion Criteria: Subjects meeting any of these criteria will not be enrolled in the study:

  • Employees of FCRL or PBL
  • Not willing to use contraceptives (preferably condoms) during sexual activity for the period of 3 months from the date of check-in
  • History of hypersensitivity and / or intolerance to Dipeptidyl peptidase (DPP)-IV inhibitors or any other related compounds.
  • History of anaphylaxis to drugs or allergic reactions in general, which the Investigator considers may affect the outcome of the study.
  • Clinically abnormal ECG and Chest X-ray.
  • Physical findings: clinically relevant abnormal physical findings (including body temperature) suggesting underlying pathologies or those which could interfere with the objectives of the study.
  • Gastrointestinal disorders likely to influence drug absorption including acute gastrointestinal symptoms (e.g. nausea, vomiting, diarrhoea, heart burn), preceding one week to admission.
  • Laboratory values that are significantly different than the normal reference range and/or are deemed to be of clinical significance by the investigator
  • Presence of reactive disease markers of HIV 1 and II, HBsAg,, HCV or VDRL.
  • Positive for alcohol breath test and/or urine drug screen (barbiturates, benzodiazepines, amphetamine, cocaine, opiates, tetra-hydro cannabinol).
  • Any evidence of organ dysfunction or any clinically significant deviation from the normal, in physical or clinical determinations.
  • History of Diabetes Mellitus or intake of any anti-diabetic medication
  • Diseases: relevant history of renal, hepatic, cardiovascular, respiratory, skin, haematological, endocrine, neurological or gastrointestinal diseases. History of depression, psychosis, schizophrenia or any other severe psychiatric diseases, or epilepsy, or any other illness that may interfere with the aim of the study. History of any significant illness in the 4 weeks preceding the screening
  • Medications: history of intake of any medications including over the counter medications (OTC) during the 4 weeks period prior to dosing with the IMP.
  • Investigational drug trials: participation in the evaluation of any drug in the 3 months prior to the start of the study (dosing with IMP).
  • Blood donation: Subjects who, through completion of this study, would have donated and/or lost more than 300 mL of blood in the past 12 weeks

Note: In case the blood loss is ≤ 200 mL; subject may be dosed 60 days after blood donation or last sample of the previous study

  • Regular smokers who smoke more than 10 cigarettes daily or have difficulty abstaining from smoking for the duration of each study period.
  • History of drug dependence or alcoholics
Male
18 Years to 60 Years
Yes
Contact: Dr Deepak C Chilkoti +91-129-4090 900 Deepak.chilkoti@fortis-cro.com
India
 
NCT01554293
PBL/CR/2011/05/CT
Yes
Panacea Biotec Ltd
Panacea Biotec Ltd
Not Provided
Principal Investigator: Dr Deepak C Chilkoti Head-Clinical Operations
Panacea Biotec Ltd
May 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP