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  1. Article ; Online: A multi-centre, post-marketing surveillance study of Vi polysaccharide-tetanus toxoid conjugate vaccine (Typbar TCV®) in India.

    Reddy, Raghu / Reddy, Bhargav / Sarangi, Vamshi / Reddy, Siddharth / Ella, Raches / Vadrevu, Krishna Mohan

    Human vaccines & immunotherapeutics

    2021  Volume 18, Issue 1, Page(s) 1947761

    Abstract: A typhoid Vi capsular-polysaccharide tetanus toxoid conjugate vaccine (Typbar-TCV®) was recommended by the World Health Organization for use in children >6 months of age. The present post-marketing surveillance study was intended to assess the clinical ... ...

    Abstract A typhoid Vi capsular-polysaccharide tetanus toxoid conjugate vaccine (Typbar-TCV®) was recommended by the World Health Organization for use in children >6 months of age. The present post-marketing surveillance study was intended to assess the clinical safety of approximately 11 million doses of TCV sold till 2019 in a diverse age range Indian population. Both active and passive post-marketing surveillance studies were conducted at multiple centers. Active surveillance was performed in two periods, Period-I: February to October 2016, Period-II: April 2017 to October 2018. In Period-II, the Brighton Collaboration Criteria adverse event case definitions were used. Passive surveillance was performed from February 2016 to December 2019 through voluntary reporting by pediatricians across India. During the active surveillance, 1147 adverse events were reported among 4,991 (23.0%) subjects in Period-I, and 596 adverse events among 3898 (21.3%) subjects in Period-II. The most frequent adverse events were fever (9.2% and 12.02%in Periods I and II, respectively), pain at the injection site (8.3% and 7.33%), and swelling (4.0% and 1.93%). No serious adverse events (SAEs) were reported during either Period. Passive surveillance revealed 235 adverse events, including 25 SAEs requiring hospitalization, of which two were due to typhoid fever. All the events mentioned above occurred within one week of vaccination, and all the subjects have recovered from AEs with medications. All reported adverse events resolved with no clinical sequelae. Observations in this study are consistent with the pre-licensure studies with no additional safety signals detected, confirming that Typbar-TCV® is safe.
    MeSH term(s) Child ; Humans ; India/epidemiology ; Product Surveillance, Postmarketing ; Tetanus Toxoid/adverse effects ; Typhoid Fever/epidemiology ; Typhoid-Paratyphoid Vaccines ; Vaccines, Conjugate
    Chemical Substances Tetanus Toxoid ; Typhoid-Paratyphoid Vaccines ; Vaccines, Conjugate
    Language English
    Publishing date 2021-07-09
    Publishing country United States
    Document type Journal Article ; Multicenter Study ; Research Support, Non-U.S. Gov't
    ZDB-ID 2664176-8
    ISSN 2164-554X ; 2164-5515
    ISSN (online) 2164-554X
    ISSN 2164-5515
    DOI 10.1080/21645515.2021.1947761
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Neutralization of VUI B.1.1.28 P2 variant with sera of COVID-19 recovered cases and recipients of Covaxin an inactivated COVID-19 vaccine.

    Sapkal, Gajanan / Yadav, Pragya D / Ella, Raches / Abraham, Priya / Patil, Deepak Y / Gupta, Nivedita / Panda, Samiran / Mohan, V Krishna / Bhargava, Balram

    Journal of travel medicine

    2021  Volume 28, Issue 7

    MeSH term(s) Antibodies, Neutralizing ; COVID-19 ; COVID-19 Vaccines ; Humans ; Neutralization Tests ; SARS-CoV-2
    Chemical Substances Antibodies, Neutralizing ; COVID-19 Vaccines
    Language English
    Publishing date 2021-05-17
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1212504-0
    ISSN 1708-8305 ; 1195-1982
    ISSN (online) 1708-8305
    ISSN 1195-1982
    DOI 10.1093/jtm/taab077
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Booster dose of the inactivated COVID-19 vaccine BBV152 (Covaxin) enhances the neutralizing antibody response against Alpha, Beta, Delta and Omicron variants of concern.

    Deshpande, Gururaj Rao / Yadav, Pragya D / Abraham, Priya / Nyayanit, Dimpal A / Sapkal, Gajanan N / Shete, Anita M / Gupta, Nivedita / Vadrevu, Krishna Mohan / Ella, Raches / Panda, Samiran / Bhargava, Balram

    Journal of travel medicine

    2022  Volume 29, Issue 3

    MeSH term(s) Antibodies, Neutralizing ; COVID-19/prevention & control ; COVID-19 Vaccines ; Humans ; SARS-CoV-2 ; Vaccines, Inactivated
    Chemical Substances Antibodies, Neutralizing ; COVID-19 Vaccines ; Vaccines, Inactivated
    Language English
    Publishing date 2022-03-23
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1212504-0
    ISSN 1708-8305 ; 1195-1982
    ISSN (online) 1708-8305
    ISSN 1195-1982
    DOI 10.1093/jtm/taac039
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Immunogenicity and reactogenicity of an inactivated SARS-CoV-2 vaccine (BBV152) in children aged 2-18 years: interim data from an open-label, non-randomised, age de-escalation phase 2/3 study.

    Vadrevu, Krishna Mohan / Reddy, Siddharth / Jogdand, Harsh / Ganneru, Brunda / Mirza, Nizam / Tripathy, Virendra Nath / Singh, Chandramani / Khalatkar, Vasant / Prasanth, Siddaiah / Rai, Sanjay / Ella, Raches / Blackwelder, William / Prasad, Sai / Ella, Krishna

    The Lancet. Infectious diseases

    2022  Volume 22, Issue 9, Page(s) 1303–1312

    Abstract: Background: Despite having milder symptoms than adults, children are still susceptible to and can transmit SARS-CoV-2. Vaccination across all age groups is therefore necessary to curtail the pandemic. Among the available COVID-19 vaccine platforms, an ... ...

    Abstract Background: Despite having milder symptoms than adults, children are still susceptible to and can transmit SARS-CoV-2. Vaccination across all age groups is therefore necessary to curtail the pandemic. Among the available COVID-19 vaccine platforms, an inactivated vaccine platform has the advantage of excellent safety profile across all age groups; hence, we conducted an age de-escalation study to assess the safety, reactogenicity, and immunogenicity of an inactivated COVID-19 vaccine, BBV152 (COVAXIN; Bharat Biotech International, Hyderabad, India), in children aged 2-18 years.
    Methods: In this phase 2/3 open-label, non-randomised, multicentre study done in six hospitals in India, healthy children (male or female) aged 2-18 years were eligible for inclusion into the study. Children who had positive SARS-CoV-2 nucleic acid and serology tests at baseline, or any history of previous SARS-CoV-2 infection, or with known immunosuppressive condition were excluded. Children were sequentially enrolled into one of three groups (>12 to ≤18 years [group 1], >6 to 12 years [group 2], or ≥2 to 6 years [group 3]) and administered with adult formulation of BBV152 as two 0·5 mL intramuscular doses on days 0 and 28. Co-primary endpoints were solicited adverse events for 7 days post-vaccination and neutralising antibody titres on day 56, 28 days after the second dose. Immunogenicity endpoints were compared with Biodefense and Emerging Infections, Research Resources Repository (BEI) reference serum samples and from adults who received two doses of BBV152 in the same schedule in a previously reported phase 2 study. The trial is registered with the Clinical Trials Registry, India (CTRI/2021/05/033752) and ClinicalTrials.gov (NCT04918797).
    Findings: From May 27, 2021, to July 10, 2021, we enrolled 526 children sequentially into groups 1 (n=176), 2 (n=175), and 3 (n=175). Vaccination was well tolerated, with no differences in reactogenicity between the three age groups, and no serious adverse events, deaths, or withdrawals due to an adverse event. Local reactions mainly consisted of mild injection site pain in 46 (26%) of 176 participants in group 1, 61 (35%) of 175 in group 2, and 39 (22%) of 175 in group 3 after dose 1; and 39 (22%) of 176 in group 1, 43 of 175 (25%) in group 2, and 14 of 175 (8%) in group 3 after dose 2; there were no cases of severe pain and few reports of other local reactions. After dose 1, the most frequent solicited systemic adverse event was mild-to-moderate fever, reported in eight (5%) of 176 participants in group 1, 17 (10%) of 175 in group 2, and 22 (13%) of 175 in group 3. No case of severe fever was reported, and rates of all fever were all 4% or less after dose 2. Geometric mean titres (GMTs) of microneutralisation antibodies at day 56 in groups 1 (138·8 [95% CI 111·0-173·6]), 2 (137·4 [99·1-167·5]), and 3 (197·6 [176·4-221·4]) were similar to titres in vaccinated adults (160·1 [135·8-188·8]) and with BEI reference serum samples (103·3 [50·3-202·1]). Similar results were obtained using the plaque reduction neutralisation test (PRNT), in which 166 (95%) of 175 participants in group 1, 165 (98%) of 168 in group 2, and 169 (98%) of 172 in group 3 seroconverted at day 56. The GMT ratio of PRNT titres in children and adults was 1·76 (95% CI 1·32-2·33), indicating a superior response in children compared with adults.
    Interpretation: BBV152 was well tolerated in children aged 2-18 years, and induced higher neutralising antibody responses than those observed in adults, in whom the efficacy (ie, the prevention or decrease in the severity of COVID-19 infection) has been demonstrated.
    Funding: Bharat Biotech International.
    MeSH term(s) Adolescent ; Antibodies, Neutralizing ; Antibodies, Viral ; COVID-19 ; COVID-19 Vaccines ; Child ; Child, Preschool ; Double-Blind Method ; Female ; Humans ; Immunogenicity, Vaccine ; Male ; Pain ; SARS-CoV-2 ; Vaccines, Inactivated ; Viral Vaccines
    Chemical Substances Antibodies, Neutralizing ; Antibodies, Viral ; COVID-19 Vaccines ; Vaccines, Inactivated ; Viral Vaccines
    Language English
    Publishing date 2022-06-16
    Publishing country United States
    Document type Clinical Trial, Phase II ; Clinical Trial, Phase III ; Journal Article ; Multicenter Study ; Research Support, Non-U.S. Gov't
    ZDB-ID 2061641-7
    ISSN 1474-4457 ; 1473-3099
    ISSN (online) 1474-4457
    ISSN 1473-3099
    DOI 10.1016/S1473-3099(22)00307-3
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Neutralization of Variant Under Investigation B.1.617.1 With Sera of BBV152 Vaccinees.

    Yadav, Pragya D / Sapkal, Gajanan N / Abraham, Priya / Ella, Raches / Deshpande, Gururaj / Patil, Deepak Y / Nyayanit, Dimpal A / Gupta, Nivedita / Sahay, Rima R / Shete, Anita M / Panda, Samiran / Bhargava, Balram / Mohan, V Krishna

    Clinical infectious diseases : an official publication of the Infectious Diseases Society of America

    2021  Volume 74, Issue 2, Page(s) 366–368

    MeSH term(s) Antibodies, Neutralizing ; Antibodies, Viral ; Humans ; Neutralization Tests
    Chemical Substances Antibodies, Neutralizing ; Antibodies, Viral
    Language English
    Publishing date 2021-05-10
    Publishing country United States
    Document type Letter ; Research Support, Non-U.S. Gov't
    ZDB-ID 1099781-7
    ISSN 1537-6591 ; 1058-4838
    ISSN (online) 1537-6591
    ISSN 1058-4838
    DOI 10.1093/cid/ciab411
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: A randomized, open-labelled, non-inferiority phase 4 clinical trial to evaluate the immunogenicity and safety of the live, attenuated, oral rotavirus vaccine, ROTAVAC® in comparison with a licensed rotavirus vaccine in healthy infants

    Ella, Raches / Babji, Sudhir / Blackwelder, William C / Ciarlet, Max / Vadrevu, Krishna Mohan

    Vaccine. 2019 July 18, v. 37, no. 31

    2019  

    Abstract: ROTAVAC® (nHRV), derived naturally from the human 116E rotavirus (RV) neonatal strain, was licensed in India in 2015 based on promising results of a phase 3, safety and efficacy vaccine trial. As a pre-requisite for WHO prequalification, we compared the ... ...

    Abstract ROTAVAC® (nHRV), derived naturally from the human 116E rotavirus (RV) neonatal strain, was licensed in India in 2015 based on promising results of a phase 3, safety and efficacy vaccine trial. As a pre-requisite for WHO prequalification, we compared the immunogenicity and safety of ROTAVAC® to those of a WHO-prequalified, Rotarix®.We conducted a multicentre, open-labeled, randomized phase 4 clinical trial where 464 infants, 6–8 weeks of age were equally randomized to receive as licensed, the complete regimen of ROTAVAC® (3 doses; Group I) or Rotarix® (2 doses; Group II). Antibody responses (serum anti-RV Immunoglobulin A [IgA]) were measured by enzyme-linked immunosorbent assay (ELISA). The primary analysis was an assessment of non-inferiority of ROTAVAC® to Rotarix® for geometric mean concentration (GMC) for infants who received the complete regimen of either vaccine.The GMC for Group I was 20.4 (95%CI: 17.6, 23.6) and that for Group II was 24.8 (95%CI: 20.3, 30.3), the GMC ratio was 0.82 (95% CI: 0.64, 1.05), thus meeting the non-inferiority criterion. Site-wise analysis of GMC titres revealed that one site had a peculiar pre-vaccination titre affecting only ROTAVAC® post-vaccination GMCs. Seroconversion rates were 35.3% (95%CI: 29.0, 41.9) and 31.0% (95%CI: 25.1, 37.4) for Groups I and Group II, respectively. There was no substantive difference in safety profiles between both vaccines.The complete regimen of ROTAVAC® demonstrated immunological non-inferiority to the complete regimen of Rotarix® with a clinically acceptable safety profile. Because the demand for RV vaccines is increasing as more countries are expanding their immunization schedules, the lack of need of a buffering agent, low dose volume (0.5 mL), non-interference with other concomitantly administered vaccines, and conformance with WHO-prequalification requirements provide ROTAVAC® the potential for widespread global usage. Post completion of this study, ROTAVAC® is now a WHO-prequalified vaccine.Clinical Trials Registration: (CTRI Number: CTRI/2015/12/006428).
    Keywords antibodies ; blood serum ; clinical trials ; enzyme-linked immunosorbent assay ; geometry ; humans ; immunization ; immunogenicity ; immunoglobulin A ; infants ; Rotavirus ; seroconversion ; vaccines ; India
    Language English
    Dates of publication 2019-0718
    Size p. 4407-4413.
    Publishing place Elsevier Ltd
    Document type Article
    ZDB-ID 605674-x
    ISSN 1873-2518 ; 0264-410X
    ISSN (online) 1873-2518
    ISSN 0264-410X
    DOI 10.1016/j.vaccine.2019.05.069
    Database NAL-Catalogue (AGRICOLA)

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  7. Article ; Online: Persistence of Immune Responses With an Inactivated Japanese Encephalitis Single-Dose Vaccine, JENVAC and Interchangeability With a Live-Attenuated Vaccine.

    Vadrevu, Krishna Mohan / Potula, Venugopal / Khalatkar, Vasant / Mahantshetty, Niranjana S / Shah, Atish / Ella, Raches

    The Journal of infectious diseases

    2019  Volume 222, Issue 9, Page(s) 1478–1487

    Abstract: Background: This study reports immunogenicity, safety, and interchangeability of a single-dose, inactivated, Vero-cell derived, JENVAC to the live-attenuated SA 14-14-2 vaccine in healthy children.: Methods: This phase 4, multicenter, open-label, ... ...

    Abstract Background: This study reports immunogenicity, safety, and interchangeability of a single-dose, inactivated, Vero-cell derived, JENVAC to the live-attenuated SA 14-14-2 vaccine in healthy children.
    Methods: This phase 4, multicenter, open-label, randomized, control trial enrolled 360 children who were equally randomized to receive a single dose of either JENVAC or SA 14-14-2. Children were followed at various time points, until 2 years (day 720) postvaccination, upon which a subset from each group was divided and allocated to a receive a booster dose or the other vaccine.
    Results: At all time points, immunological measures were statistically higher in the JENVAC group. In the interchangeability study, children receiving 2 doses of JENVAC reported significantly higher response compared with 2 doses of SA 14-14-2. No difference in adverse events was observed. These corroborate with excellent seroprotection after the first dose of an earlier JENVAC study.
    Conclusions: A single-dose vaccination with JENVAC induces protective titers that persist up to 1 year. We report appreciable interchangeability between both vaccines, with JENVAC/JENVAC combination exhibiting the highest immune response. JENVAC is now licensed as a single-dose Japanese encephalitis vaccine.
    MeSH term(s) Adolescent ; Age Factors ; Child ; Child, Preschool ; Encephalitis Virus, Japanese/immunology ; Encephalitis, Japanese/immunology ; Encephalitis, Japanese/prevention & control ; Female ; Humans ; Infant ; Japanese Encephalitis Vaccines/administration & dosage ; Japanese Encephalitis Vaccines/immunology ; Japanese Encephalitis Vaccines/therapeutic use ; Male ; Neutralization Tests ; Single-Blind Method ; Vaccines, Attenuated ; Vaccines, Inactivated
    Chemical Substances Japanese Encephalitis Vaccines ; Vaccines, Attenuated ; Vaccines, Inactivated
    Language English
    Publishing date 2019-12-17
    Publishing country United States
    Document type Clinical Trial, Phase IV ; Journal Article ; Multicenter Study ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
    ZDB-ID 3019-3
    ISSN 1537-6613 ; 0022-1899
    ISSN (online) 1537-6613
    ISSN 0022-1899
    DOI 10.1093/infdis/jiz672
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Inactivated COVID-19 vaccine BBV152/COVAXIN effectively neutralizes recently emerged B.1.1.7 variant of SARS-CoV-2.

    Sapkal, Gajanan N / Yadav, Pragya D / Ella, Raches / Deshpande, Gururaj R / Sahay, Rima R / Gupta, Nivedita / Vadrevu, Krishna Mohan / Abraham, Priya / Panda, Samiran / Bhargava, Balram

    Journal of travel medicine

    2021  Volume 28, Issue 4

    MeSH term(s) Antibodies, Neutralizing ; Antibodies, Viral ; COVID-19/prevention & control ; COVID-19/virology ; COVID-19 Vaccines/immunology ; Humans ; SARS-CoV-2 ; Vaccines, Inactivated/immunology
    Chemical Substances Antibodies, Neutralizing ; Antibodies, Viral ; COVID-19 Vaccines ; Vaccines, Inactivated
    Language English
    Publishing date 2021-03-27
    Publishing country England
    Document type Journal Article
    ZDB-ID 1212504-0
    ISSN 1708-8305 ; 1195-1982
    ISSN (online) 1708-8305
    ISSN 1195-1982
    DOI 10.1093/jtm/taab051
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Neutralization of Beta and Delta variant with sera of COVID-19 recovered cases and vaccinees of inactivated COVID-19 vaccine BBV152/Covaxin.

    Yadav, Pragya D / Sapkal, Gajanan N / Ella, Raches / Sahay, Rima R / Nyayanit, Dimpal A / Patil, Deepak Y / Deshpande, Gururaj / Shete, Anita M / Gupta, Nivedita / Mohan, V Krishna / Abraham, Priya / Panda, Samiran / Bhargava, Balram

    Journal of travel medicine

    2021  Volume 28, Issue 7

    MeSH term(s) Antibodies, Neutralizing ; COVID-19 ; COVID-19 Vaccines ; Humans ; SARS-CoV-2
    Chemical Substances Antibodies, Neutralizing ; COVID-19 Vaccines
    Language English
    Publishing date 2021-07-06
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1212504-0
    ISSN 1708-8305 ; 1195-1982
    ISSN (online) 1708-8305
    ISSN 1195-1982
    DOI 10.1093/jtm/taab104
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: A randomized, open-labelled, non-inferiority phase 4 clinical trial to evaluate the immunogenicity and safety of the live, attenuated, oral rotavirus vaccine, ROTAVAC® in comparison with a licensed rotavirus vaccine in healthy infants.

    Ella, Raches / Babji, Sudhir / Ciarlet, Max / Blackwelder, William C / Vadrevu, Krishna Mohan

    Vaccine

    2019  Volume 37, Issue 31, Page(s) 4407–4413

    Abstract: Background: ROTAVAC® (nHRV), derived naturally from the human 116E rotavirus (RV) neonatal strain, was licensed in India in 2015 based on promising results of a phase 3, safety and efficacy vaccine trial. As a pre-requisite for WHO prequalification, we ... ...

    Abstract Background: ROTAVAC® (nHRV), derived naturally from the human 116E rotavirus (RV) neonatal strain, was licensed in India in 2015 based on promising results of a phase 3, safety and efficacy vaccine trial. As a pre-requisite for WHO prequalification, we compared the immunogenicity and safety of ROTAVAC® to those of a WHO-prequalified, Rotarix®.
    Methods: We conducted a multicentre, open-labeled, randomized phase 4 clinical trial where 464 infants, 6-8 weeks of age were equally randomized to receive as licensed, the complete regimen of ROTAVAC® (3 doses; Group I) or Rotarix® (2 doses; Group II). Antibody responses (serum anti-RV Immunoglobulin A [IgA]) were measured by enzyme-linked immunosorbent assay (ELISA). The primary analysis was an assessment of non-inferiority of ROTAVAC® to Rotarix® for geometric mean concentration (GMC) for infants who received the complete regimen of either vaccine.
    Results: The GMC for Group I was 20.4 (95%CI: 17.6, 23.6) and that for Group II was 24.8 (95%CI: 20.3, 30.3), the GMC ratio was 0.82 (95% CI: 0.64, 1.05), thus meeting the non-inferiority criterion. Site-wise analysis of GMC titres revealed that one site had a peculiar pre-vaccination titre affecting only ROTAVAC® post-vaccination GMCs. Seroconversion rates were 35.3% (95%CI: 29.0, 41.9) and 31.0% (95%CI: 25.1, 37.4) for Groups I and Group II, respectively. There was no substantive difference in safety profiles between both vaccines.
    Conclusions: The complete regimen of ROTAVAC® demonstrated immunological non-inferiority to the complete regimen of Rotarix® with a clinically acceptable safety profile. Because the demand for RV vaccines is increasing as more countries are expanding their immunization schedules, the lack of need of a buffering agent, low dose volume (0.5 mL), non-interference with other concomitantly administered vaccines, and conformance with WHO-prequalification requirements provide ROTAVAC® the potential for widespread global usage. Post completion of this study, ROTAVAC® is now a WHO-prequalified vaccine.
    Clinical trials registration: (CTRI Number: CTRI/2015/12/006428).
    MeSH term(s) Antibodies, Viral/blood ; Antibodies, Viral/immunology ; Diarrhea, Infantile/prevention & control ; Diarrhea, Infantile/virology ; Female ; Humans ; Immunization Schedule ; Immunogenicity, Vaccine ; India/epidemiology ; Infant ; Infant, Newborn ; Male ; Outcome Assessment, Health Care ; Rotavirus/immunology ; Rotavirus Infections/prevention & control ; Rotavirus Vaccines/administration & dosage ; Rotavirus Vaccines/adverse effects ; Rotavirus Vaccines/immunology ; Seroepidemiologic Studies ; Vaccination
    Chemical Substances Antibodies, Viral ; Rotavirus Vaccines
    Language English
    Publishing date 2019-06-06
    Publishing country Netherlands
    Document type Clinical Trial, Phase IV ; Journal Article ; Multicenter Study ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
    ZDB-ID 605674-x
    ISSN 1873-2518 ; 0264-410X
    ISSN (online) 1873-2518
    ISSN 0264-410X
    DOI 10.1016/j.vaccine.2019.05.069
    Database MEDical Literature Analysis and Retrieval System OnLINE

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