Serum Institute Of India Gets CDSCO Panel Nod To study Dengue Tetravalent Vaccine
New Delhi: Vaccine major Serum Institute of India has got a go-ahead from the Subject Expert Committee (SEC) functional under Central Drug Standard Control Organization (CDSCO) to conduct a Phase I/II clinical trial of Dengue Tetravalent Vaccine (Live, Attenuated).
This came after the Serum Institute of India presented the revised protocol for the grant of permission to conduct Phase I/II clinical trial of the Dengue Tetravalent Vaccine (Live, Attenuated).
Dengue Tetravalent Vaccine (Live, Attenuated) provides protection against fever and hospitalization resulting from dengue disease caused by any of the 4 dengue virus serotypes. Side effects are mostly mild to moderate in severity and disappear within a few days.
Dengue is a mosquito-borne tropical disease caused by the dengue virus, leading to mild, flu-like symptoms in most people. However, a small number of patients develop severe disease, with potentially fatal bleeding and organ damage.
Dengue spreads to people through the bite of an infected mosquito. It does not spread directly from person to person. However, a pregnant person can pass the infection on to the baby. In rare cases, it can spread through a blood transfusion, organ transplant, or needle stick injury.
This vaccine contains attenuated (weakened) versions of dengue virus serotypes (varieties) 1, 2, 3, and 4.
Earlier, the Medical Dialogues Team had reported that at the SEC meeting for Vaccine held on 23rd March 2023, the committee had recommended the firm revise the Phase I/II clinical trial protocol as below:
1. The trial design should be seamless with Phase I followed by Phase II along with DSMB review after Phase-I. The clinical trial report of Phase-I with DSMB recommendations should be submitted before the initiation of Phase II.
2. The clinical trial should be stratified and conducted in adult subjects initially and then in pediatric subjects.
3. The inclusion of seropositive and seronegative subjects should be clearly defined in the protocol.
In accordance with the above, at the recent SEC meeting on 18th July 2023, the Serum Institute of India presented the revised protocol for the grant of permission to conduct a Phase I/II clinical trial of the Dengue Tetravalent Vaccine (Live, Attenuated).
After detailed deliberation, the committee recommended the grant of permission to conduct Phase I/II clinical trial of the Dengue Tetravalent Vaccine (Live, Attenuated) as per the presented protocol.
Also Read:Exemed Pharma Gets CDSCO Panel Nod To Study FDC of Montelukast, Bilastine
Disclaimer: This website is primarily for healthcare professionals. The content here does not replace medical advice and should not be used as medical, diagnostic, endorsement, treatment, or prescription advice. Medical science evolves rapidly, and we strive to keep our information current. If you find any discrepancies, please contact us at corrections@medicaldialogues.in. Read our Correction Policy here. Nothing here should be used as a substitute for medical advice, diagnosis, or treatment. We do not endorse any healthcare advice that contradicts a physician's guidance. Use of this site is subject to our Terms of Use, Privacy Policy, and Advertisement Policy. For more details, read our Full Disclaimer here.
NOTE: Join us in combating medical misinformation. If you encounter a questionable health, medical, or medical education claim, email us at factcheck@medicaldialogues.in for evaluation.