WORLD'S & INDIA'S FIRST -1st DISCOVER COVID-19 VACCINE FOR CHILDRENS : ZYCOV-D

GLOBALLY DISCOVERD FOR CHILDREN 
 
AGE GROUP 12 Yrs and ABOVE : ZYCOV -D



ZYDUSCADILA  is a Leading INDIAN Multinational Drugs Manufacturing Company, Located at Ahmedabad,  Gujrat, India. Fully integrated Globally Health Care Products Provider and Generic Drugs. Company was Established in 1952 by RAMANBHAI PATEL with his Business Partner INDRAVADAN MODI . It ranked 100th in the Fortune INDIA 500 list in 2020.

In 1995 the PATEL and MODI families Split and The Modi family's was moved in to a new Company called  CADILA PHARMACEUTICALS LTD and Company became the Patel families holding Company.

In 2015 the Company  acquired another Indian Pharmaceutical Company GERMAN REMEDIES. On june 25th 2007,the Company acquired QUIMICA e FARMACEUTICA NIKKHO DO BRASIL  LTD.

In 2010, CADILA HEALTHCARE Received a  WELLCOME TRUST Award under the R&D for Affordable  Healthcare in  INDIA  initiate The world's first  ADALIMUMAB BIOSIMILAR  under the brand name EXEMPTA at 1/5 the Originator's Price. Company has also Launched its first research based drug molecule Sarogliter in treatment of  DIABETIC DYSLIPIDEMUA" under brand name  LIPAGLYN. SOVIHEP is the first  SOFOSBUVIR brand launched in INDIA in the Year 2015.

ZYDUS CADILA  is one of the Oldest Indian Formulations player of the market and  Prominent Pharmaceutical Manufacture Company in INDIA. ZYDUS CADILA  is improving its presence in the Market Share Continuously and Company Manufacturing Both pharmaceutical  Products for HUMAN'S& ANIMAL'S.

ZYDUS CADILA was Manufactured , In the year 2019, INJECTABLE KETOROLAC Tromethamine due to his 'MICROBIAL' Growth and Permitted by USFDA to initiate Clinical Trials for CANCER Patients. Company develops and manufactures a Large Range of Pharmaceuticals, Herbals, Skincare and other Products. Company Start from 2015, Having Concluded a Voluntarily License Agreement with GILEAD and also Products the GENERICS for  HEPATITIS C  Treatments. The Company has three places in INDIA, For Manufacturing of  ACTIVE PHARMACEUTICAL INGREDIENTS  

1. VARODARA 

2. ANKLESHWAR 

3. PATALGANGA


The Company decided to develop a  DNA PLASMID  Based  COVID -19 VACCINE  at their Vaccine Technology Centre  VTC in Ahmedabad and able to Pass the Pre- Clinical trials on Animals Model Successfully and Phase -I trials of the Vaccine  Started From In JULY - 2020 and Continued to until OCTOBER -2020. The Vaccine was Tested on 48 healthy Peoples in the 18-55 Years of age range and after 28 days between each of the 3rd 'DOSES' and  VTC was found  the Vaccine to be  SAFE & WELL TOLERATED and IMMUNOGENIC . 2ND Phase trials of the Vaccine from 6th AUGUST - 2021 With THOUSANDS of individuals as part of the Adaptive PHASE -  I & II  for MULTI-CENTRIC, DOSE- ESCALATION, RANDOMISED, DOBLE-BLIND . Placebo Controlled Method and Company was reported PH-II trials were Completed by NOVEMBER - 2020.


The Company Announced the Test of Vaccines with 30thousands Patients PHASE -III trial in November 2020 and reported in JAN-2021.The Drugs Controller General of INDIA, granted Permission to Conduct the trials for 28,216 Indian in the age of 12-99 group and  One thousands Individuals were in the 12-18 age group. The Company applied to DGCI  for Seeking Approval of RESTRICTED USE IN EMERGENCY SITUATION on  AUGUST-2021.The Export Committee of the  CENTRAL DRUGS STANDARD CONTROL ORGANISATION  recommended that the 'DGCI' grant the Approval on the same day

The Company got Permission to Conduct HUMAN TRIALS of the Developmental for COVID-19 VACCINE in 'JULY-2020', the named as ZYCOV-D from the DGCI , Drugs Controller General of India.




ZYCOV-D is a DNA Plasmid- Based Vaccine COVID-19, Developed by CADILA HEALTHCARE  with supported from the Biotechnology Industry Research Assistance Council for  Emergency Approval to use in  INDIA and The Vaccine is given as an   INTRADERMAL INJECTION  using a Spring Powered  JET INJECTOR. Company also Reported the  EFFICACY  to be 66.6 Percent against SYMPTOMATIC COVID-19 and Hundred percent against Moderate or Severe Diseases in its Interim Analysis of Phase-3 Trials.

The COVID-19 VACCINE  ZYCOV-D, Contains a DNA PLASMID VECTOR ,That Carries the gene Encoding the  SPIKE PROTEIN  of  SARS-COV-2 , As with other DNA VACCINES  the Recipients Cells then Produce the SPIKE  PROTEIN, ELICITING     To Protective  IMMUNE  response.

The enterprise at ultimate DISCOVERD  the WORLD'S & INDIA'S FIRST  Needle unfastened PLASMID DNA COVID-19, Vaccine for Adolescents withinside the age organization of 12-18 and Plans directly to Seek  APPROVED  for TWO DOSE  regimen.

VACCINE DESCRIPTION : 

1. Target             : SARS-Cov-2

2. Vaccine Type :  DNA

CLINICAL DATA  :   

1. Routes of Administration 

2. ATC Code          :  None

LEGAL STATUS   :  List of ZYCOV-D COVID-19-                                                     VACCINE Authorizations.

IDENTIFIERS         :  Drug Bank Accession Number-                                                DB15892





In twentieth AUGUST - FRIDAY- finally  Approval  and Declare to Emergency use in INDIA  from, The INDIAN DRUG REGULATOR'S SUBJECT EXPERT COMMITTEE Approval  to ZYDUS CADILA's COVID-19 VACCINE-- ZYCOV - D  for THREE DOSE  and The Expert Committee stated If  Company ZYDUS Required to Submit any extra files for the 2-DOSE Regimen of its VACCINE . Now Very accurate NEWS for all Global To be  SAFE &SECURE for our KIDS Life.


Tags

Post a Comment

0 Comments
* Please Don't Spam Here. All the Comments are Reviewed by Admin.
Responsive ads
Responsive Ads
Responsive ads

#buttons=(Accept !) #days=(20)

Our website uses cookies to enhance your experience. Learn More
Accept !