Die an Menschen getesteten Impfstoffkandidaten gegen COVID-19 sind unten auf dieser Seite aufgelistet.

Bis heute hat der Bund mit fünf Herstellern Verträge abgeschlossen: Moderna (in Zukunft insgesamt 20,5 Millionen Dosen), Pfizer/BioNTech (ca. 6 Millionen Dosen), AstraZeneca (ca. 5,3 Millionen Dosen) und in Zukunft Curevac (5 Millionen Dosen) sowie Novavax (6 Millionen Dosen). Auf diese Weise wird sichergestellt, dass auch bei Lieferschwierigkeiten genügend Dosen eines zugelassenen Impfstoffs für die Bevölkerung zur Verfügung stehen. Der Bund verhandelt weiterhin mit verschiedenen Herstellern, da die weitere Entwicklung der Pandemie schwer abzuschätzen ist.

Für diese Impfstoffe sind folgende wissenschaftliche Publikationen (peer-reviewed) und/oder Medienmitteilungen verfügbar.

 

mRNA-1273 (RNAm Impfstoff, Moderna et National Institute of Allergy and Infectious Diseases und Moderna)

An mRNA Vaccine against SARS-CoV-2 — Preliminary Report (New England Journal of Medicine, 14.7.2020)

Safety and Immunogenicity of SARS-CoV-2 mRNA-1273 Vaccine in Older Adults (New England Journal of Medicine, 29.9.2020)

Moderna Announces Primary Efficacy Analysis in Phase 3 COVE Study for Its COVID-19 Vaccine Candidate and Filing Today with U.S. FDA for Emergency Use Authorization (30.11.2020)

Durability of Responses after SARS-CoV-2 mRNA-1273 Vaccination (New England Journal of Medicine, 4.12.2020)

Efficacy and Safety of the mRNA-1273 SARS-CoV-2 Vaccine (New England Journal of Medicine, 30.12.2020)

A preliminary report of a randomized controlled phase 2 trial of the safety and immunogenicity of mRNA-1273 SARS-CoV-2 vaccine (Vaccine, 9.2.2021)

Antibody Persistence through 6 Months after the Second Dose of mRNA-1273 Vaccine for Covid-19 (New England Journal of Medicine, 6.4.2021)

Neutralization of SARS-CoV-2 Variants B.1.429 and B.1.351 (New England Journal of Medicine, 7.4.2021)

Moderna Announces Positive Initial Booster Data Against SARS-CoV-2 Variants of Concern (Press release, 5.5.2021)

BNT162b2-Elicited Neutralization against New SARS-CoV-2 Spike Variants (New England Journal of Medicine, 12.5.2021)

 

BNT162b2 (RNAm Impfstoff, BioNTech RNA Pharmaceuticals und Pfizer)

Phase 1/2 Study to Describe the Safety and Immunogenicity of a COVID-19 RNA Vaccine Candidate (BNT162b1) in Adults 18 to 55 Years of Age: Interim Report (1.7.2020)

Phase I/II study of COVID-19 RNA vaccine BNT162b1 in adults (Nature, 12.8.2020)

COVID-19 vaccine BNT162b1 elicits human antibody and TH1 T-cell responses (Nature, 30.9.2020)

Safety and Immunogenicity of Two RNA-Based Covid-19 Vaccine Candidates (New England Journal of Medicine, 14.10.2020)

Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine (New England Journal of Medicine, 10.12.2020)

BNT162b2 mRNA Covid-19 Vaccine in a Nationwide Mass Vaccination Setting (New England Journal of Medicine, 24.2.2021)

Neutralizing Activity of BNT162b2-Elicited Serum (New England Journal of Medicine, 8.3.2021)

Pfizer and BioNTech Confirm High Efficacy and No Serious Safety Concerns Through Up to Six Months Following Second Dose in Updated Topline Analysis of Landmark COVID-19 Vaccine Study (Press release, 1.4.2021)

Neutralizing Response against Variants after SARS-CoV-2 Infection and One Dose of BNT162b2 (New England Journal of Medicine, 7.4.2021)

Safety and immunogenicity of the SARS-CoV-2 BNT162b1 mRNA vaccine in younger and older Chinese adults: a randomized, placebo-controlled, double-blind phase 1 study (Nature Medicine, 22.4.2021)

COVID-19 vaccine coverage in health-care workers in England and effectiveness of BNT162b2 mRNA vaccine against infection (SIREN): a prospective, multicentre, cohort study (Lancet, 23.4.2021)

Interim findings from first-dose mass COVID-19 vaccination roll-out and COVID-19 hospital admissions in Scotland: a national prospective cohort study (Lancet, 23.4.2021)

Vaccine side-effects and SARS-CoV-2 infection after vaccination in users of the COVID Symptom Study app in the UK: a prospective observational study (Lancet Infectious Diseases, 27.4.2021)

Impact and effectiveness of mRNA BNT162b2 vaccine against SARS-CoV-2 infections and COVID-19 cases, hospitalisations, and deaths following a nationwide vaccination campaign in Israel: an observational study using national surveillance data (Lancet, 5.5.2021)

Effectiveness of the BNT162b2 Covid-19 Vaccine against the B.1.1.7 and B.1.351 Variants (New England Journal of Medicine, 5.5.2021)

 

AZD1222 (ChAdOx1 nCoV-19) (Impfstoff-VektorAstra Zeneca und University of Oxford)

Safety and immunogenicity of the ChAdOx1 nCoV-19 vaccine against SARS-CoV-2: a preliminary report of a phase 1/2, single-blind, randomised controlled trial (The Lancet 20.7.2020)

Safety and immunogenicity of ChAdOx1 nCoV-19 vaccine administered in a prime-boost regimen in young and old adults (COV002): a single-blind, randomised, controlled, phase 2/3 trial (The Lancet, 18.11.2020)

Safety and efficacy of the ChAdOx1 nCoV-19 vaccine (AZD1222) against SARS-CoV-2: an interim analysis of four randomised controlled trials in Brazil, South Africa, and the UK (The Lancet, 8.12.2020)

T cell and antibody responses induced by a single dose of ChAdOx1 nCoV-19 (AZD1222) vaccine in a phase 1/2 clinical trial et Phase 1/2 trial of SARS-CoV-2 vaccine ChAdOx1 nCoV-19 with a booster dose induces multifunctional antibody responses (Nature Medicine, 17.12.2020)

Single-dose administration and the influence of the timing of the booster dose on immunogenicity and efficacy of ChAdOx1 nCoV-19 (AZD1222) vaccine: a pooled analysis of four randomised trials (The Lancet, 19.2.2021)

Efficacy of the ChAdOx1 nCoV-19 Covid-19 Vaccine against the B.1.351 Variant (NEJM, 16.3.2021)

Efficacy of ChAdOx1 nCoV-19 (AZD1222) vaccine against SARS-CoV-2 variant of concern 202012/01 (B.1.1.7): an exploratory analysis of a randomised controlled trial (The Lancet, 30.3.2021)

Thromboembolism and the Oxford–AstraZeneca COVID-19 vaccine: side-effect or coincidence? (The Lancet, 30.3.2021)

Thrombosis and Thrombocytopenia after ChAdOx1 nCoV-19 Vaccination (New England Journal of Medicine, 9.4.2021)

Thrombotic Thrombocytopenia after ChAdOx1 nCov-19 Vaccination (New England Journal of Medicine, 9.4.2021)

Interim findings from first-dose mass COVID-19 vaccination roll-out and COVID-19 hospital admissions in Scotland: a national prospective cohort study (Lancet, 23.4.2021)

Vaccine side-effects and SARS-CoV-2 infection after vaccination in users of the COVID Symptom Study app in the UK: a prospective observational study (Lancet Infectious Diseases, 27.4.2021)

 

Die Impfstoffe von Moderna, Pfizer/BioNTech und AstraZeneca sind bereits in einigen Ländern zugelassen, eine Zusammenfassung der Zwischenergebnisse der bereits vorliegenden Phase-3-Studien für diese Impfstoffe finden Sie HIER.


CVnCoV Vaccine (RNAm Impfstoff, Curevac)
 
 
 
 
NVX-CoV2373 (rekombinierte Proteine, Novavax)

 

Andere Impfstoffe, die sich bereits in Phase 3 befinden (Wirksamkeit und Sicherheit):

Hinweis: Einige dieser Impfstoffe sind in einigen Ländern bereits zugelassen. Eine aktuelle Liste der Impfstoffe in klinischen Studien finden Sie in diesem regelmäßig aktualisierten WHO-Dokument.

 

Inactivated SARS-CoV-2 (inaktiviertes Virus, Sinovac und Butantan Institute)

Inactivated Novel Coronavirus Pneumonia (COVID-19) vaccine (inaktiviertes Virus, Hennan Provincial Center for Disease Control and Prevention und Sinopharm)

- BBIBP-CorV (inaktiviertes Virus, Beijing Institute of Biological Products Co., LTD und Laboratorio Elea Phoenix S.A.)

- Ad26.COV2.S (Impfstoff-Vektor, Janssen Vaccines & Prevention (Johnson & Johnson))

Ad5-nCoV (Impfstoff-Vektor, CanSino Biologics)

- Gam-COVID-Vac (Impfstoff-Vektor, Gamaleya Research Institute of Epidemiology and Microbiology, Health Ministry of the Russian Federation)

- Inactivated Novel Coronavirus Pneumonia (COVID-19) vaccine (Vero cells) (inaktiviertes Virus, Wuhan Provincial Center for Disease Control and Prevention)

- CoVLP (rekombinierte Proteine, Medicago)

BBV152 - COVAXIN (inaktiviertes Virus, Bharat Biotech International Ltd)

Recombinant new coronavirus vaccine (CHO cell) (rekombinierte Proteine, Anhui Zhifei Longcom Biologic Pharmacy Co., Ltd.)

- AG0302-COVID19 (DNA Impfstoff, AnGes Inc., Japan Agency for Medical Research and Development)

Inactivated SARS-CoV-2 Vaccine (inaktiviertes Virus, Chinese Academy of Medical Sciences)

- SCB-2019 (rekombinierte Proteine, Clover Biopharmaceuticals Australia)

nCov Vaccine (DNA Impfstoff, Cadila Healthcare Ltd)

- QazCovid-in (inaktiviertes Virus, Research Institute for Biological Safety Problems)

- UB-612 (rekombinierte Proteine, United Biomedical, COVAXX)

- EpiVacCorona (rekombinierte Proteine, Federal Budgetary Research Institution State Research Center of Virology and Biotechnology "Vector")

 Ständig aktualisierte Liste von Impfstoffkandidaten in Phase 3

 

Diese Impfstoffe und diejenigen, die sich noch in Phase I und/oder 2 befinden, werden im Folgenden beschrieben:

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