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CTRI Number  CTRI/2014/01/004343 [Registered on: 23/01/2014] Trial Registered Retrospectively
Last Modified On: 14/11/2018
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Vaccine 
Study Design  Randomized, Parallel Group Trial 
Public Title of Study   Clinical Study to assess the immune response and safety of Measles vaccine (Live) (Freeze-dried) of M/s Cadila Healthcare Ltd. in healthy pediatric subjects aged 9-12 months 
Scientific Title of Study   A randomized, open label, multicentric, phase II clinical trial to assess the immunogenicity and safety of Measles vaccine (Live) (Freeze-dried) of M/s Cadila Healthcare Ltd. in healthy pediatric subjects aged 9-12 months 
Trial Acronym   
Secondary IDs if Any  
Secondary ID  Identifier 
12-04ver1dated17-06-2013  Protocol Number 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Dr Ravindra Mittal 
Designation  Medical Advisor & Head - Regulatory Affairs 
Affiliation  Cadila Healthcare Ltd. 
Address  Cadila Healthcare Ltd., Zydus-PTC, Sigma Commerce Zone, B/H ISCON Temple, Near Satellite Cross Roads, Ambli-Bopal Road

Ahmadabad
GUJARAT
380015
India 
Phone  07926868926  
Fax  07926868910  
Email  r.mittal@zyduscadila.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Ravindra Mittal 
Designation  Medical Advisor & Head - Regulatory Affairs 
Affiliation  Cadila Healthcare Ltd. 
Address  Cadila Healthcare Ltd., Zydus-PTC, Sigma Commerce Zone, B/H ISCON Temple, Near Satellite Cross Roads, Ambli-Bopal Road


GUJARAT
380015
India 
Phone  07926868926  
Fax  07926868910  
Email  r.mittal@zyduscadila.com  
 
Details of Contact Person
Public Query
 
Name  Dr Jayesh Sanmukhani 
Designation  Manager – New Product Development 
Affiliation  Cadila Healthcare Ltd. 
Address  Zydus-PTC, Sigma Commerce Zone, B/H ISCON Temple, Near Satellite Cross Roads, Ambli-Bopal Road.

Ahmadabad
GUJARAT
380015
India 
Phone  07926868924  
Fax  07926868910  
Email  jayeshsanmukhani@zyduscadila.com  
 
Source of Monetary or Material Support  
Cadila Healthcare Ltd 
 
Primary Sponsor  
Name  Cadila Healthcare Ltd 
Address  Cadila Healthcare Ltd., Zydus-PTC, Sigma Commerce Zone, B/H ISCON Temple, Near Satellite Cross Roads, Ambli-Bopal Road, Ahmedabad - 380015  
Type of Sponsor  Pharmaceutical industry-Indian 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study
Modification(s)  
No of Sites = 6  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dr Bakul B Javadekar  Department of Paediatrics, SSG Hospital  Ward No. 17 (First Floor). S.S.G. Hospital, Raopura, Vadodara - 390001, Gujarat, India.
Vadodara
GUJARAT 
9925014448

bjavadekar@rediffmail.com 
Dr Nandini Malshe  Department of Pediatrics, Bharati Hospital & Research Centre, Bharati Vidyapeeth   Bharati Hospital & Research Centre, Bharati Vidyapeeth Deemed University Medical College and Hospital. Pune Satara Road, Katraj-Dhankawadi, Pune - 411 043, Maharashtra
Pune
MAHARASHTRA 
02024364308

researchpedpune@gmail.com 
Dr Baldev Prajapati  Department of Pediatrics, GCS Medical College & Hospital  GCS Medical College. Opp. DRM Office, Nr. Chamunda Bridge, Naroda Road, Ahmedabad – 380013
Ahmadabad
GUJARAT 
9824039376

baldevprajapati55@gmail.com 
Dr Uma Siddhartha Nayak   Department of Pediatrics, GMERS Medical College & Government Hospital  GMERS Medical College & General Hospital, Gotri, Vadodara 390021, Gujarat, India
Vadodara
GUJARAT 
9327214065

umasnayak@gmail.com 
Dr Rajesh N Joshi   Department of Pediatrics, GMERS Medical College and Government Hospital   GMERS Medical College, Sola. S.G. Highway, Near New Gujarat high court, Ahmedabad-380061, Gujarat, India
Ahmadabad
GUJARAT 
9879513412

rnjoshi@gmail.com 
Dr Sharad Agarkhedkar   Department of Pediatrics, Padmashree Dr. D. Y. Patil Medical college and Hospital  Padmashree Dr. D. Y. Patil Medical college and Hospital, Pimpri, Pune – 18
Pune
MAHARASHTRA 
9011090078

ashalaka@gmail.com 
 
Details of Ethics Committee
Modification(s)  
No of Ethics Committees= 6  
Name of Committee  Approval Status 
Ethics committee GMERS Medical College, Sola, S.G. Highway, Near New Gujarat High Court, Ahmedabad  Approved 
Ethics Committee- Dr. D. Y. Patil Vidyapeeth, Pune, Pimpri, Pune   Approved 
Institutional Ethics Committee (Institutional Review Board) GMERS Medical College Gotri, Gotri Road, Vadodara   Approved 
Institutional Ethics Committee Bharati Vidyapeeth Deemed University, Pune  Approved 
Institutional Ethics Committee on human Research, Medical College Baroda   Approved 
Institutional Ethics Committee, GCS Medical college, Hospital & Research Centre, Ahmedabad   Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Approved/Obtained 
 
Health Condition / Problems Studied
Modification(s)  
Health Type  Condition 
Healthy Human Volunteers  Active immunization for the prevention of Measles 
Patients  (1) ICD-10 Condition: Z23||Encounter for immunization,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Measles vaccine (Live)-Single dose (Freeze-dried) of M/s Cadila Healthcare Ltd; Measles vaccine (Live)-Multi dose (Freeze-dried) of M/s Cadila Healthcare Ltd.   Each subject will be given a single dose of 0.5ml vaccine from single dose vial given as a subcutaneous injection in the upper arm on 0 day; Each subject will be given a single dose of 0.5ml vaccine from multidose vial given as a subcutaneous injection in the upper arm on 0 day 
Comparator Agent  NIL  NIL 
 
Inclusion Criteria  
Age From  9.00 Month(s)
Age To  12.00 Month(s)
Gender  Both 
Details  1.Healthy pediatric subjects of either sex aged 9 months to 12 months.
2.Informed consent of the parents/guardians and their willingness to be followed up for at least 6 weeks after vaccination of their child.
3.Parents/guardians with adequate literacy to fill the diary cards
 
 
ExclusionCriteria 
Details  1.Subjects with a history of anaphylaxis or serious reactions to vaccines; hypersensitivity to neomycin.
2.Subjects with a history of previous measles infection or measles vaccination or if they had been exposed to measles virus within 30 days of trial commencement.
3.A history of convulsions, epilepsy or other central nervous system diseases or an acute febrile illness at the time of planned vaccination.
4.Any other parenteral vaccine administration within 30 days of initiation of the study or during the study.
5.A history of serious chronic illness, major congenital defects, immunosuppression (immunosuppressive illness or therapy).
6.Subjects who have received blood products or immunoglobulins parenterally during the preceding 3 months.
7.Subjects with any other clinically significant concurrent illness. 
 
Method of Generating Random Sequence   Computer generated randomization 
Method of Concealment   Not Applicable 
Blinding/Masking   Open Label 
Primary Outcome  
Outcome  TimePoints 
The primary immunogenicity criteria will be the
seroconversion rate for measles 
42 days
following
vaccination 
 
Secondary Outcome  
Outcome  TimePoints 
The secondary immunogenicity criteria will be the postvaccination
geometric mean titers (GMTs) of antibodies to
measles 
42 days
following
vaccination 
 
Target Sample Size   Total Sample Size="100"
Sample Size from India="100" 
Final Enrollment numbers achieved (Total)= ""
Final Enrollment numbers achieved (India)="" 
Phase of Trial   Phase 2 
Date of First Enrollment (India)   20/01/2014 
Date of Study Completion (India) Date Missing 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Date Missing 
Estimated Duration of Trial   Years="0"
Months="6"
Days="0" 
Recruitment Status of Trial (Global)
Modification(s)  
Not Applicable 
Recruitment Status of Trial (India)  Completed 
Publication Details    
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Brief Summary  

This is a randomized, open label, parallel group, multicentric, phase II clinical trial to assess the immunogenicity and safety of Measles vaccine (Live) (Freeze-dried) of M/s Cadila Healthcare Ltd. (CHL) in healthy pediatric subjects aged 9-12 months. Hundred subjects will be randomized to receive Measles vaccine from either a single dose vial or a multidose vial. A pre vaccination and a post vaccination (day 42) blood sample will be collected to determine antibody titres attained after vaccination. The primary immunogenicity criteria will be the seroconversion rate which would be estimated as follows: 1. The percentage of subjects who had been seronegative before vaccination and who developed antibody concentrations of ≥ 200 Milli International Unit (mIU)/ml for measles 42 days following vaccination. 2.  The percentage of subjects who were already seropositive for measles at the time of immunization and developed a ≥ 4 fold increase in the respective antibody titers 42 days following vaccination. The safety of the vaccine will be assessed by recording the adverse events occurring during the entire course of the study

 
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