Vaccine Manufacturing Collaborations
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Updated May 26, 2021 Cross-Border Industry Partnerships on COVID-19 Vaccines and Therapeutics Vaccines • Curevac O Celonic Wi
Updated May 26, 2021 Cross-Border Industry Partnerships on COVID-19 Vaccines and Therapeutics Vaccines • CureVac o Celonic will manufacture 100 million doses of CureVac’s vaccine at its plant in Heidelberg, Germany, providing bulk substance for 50 million doses by the end of 2021. (press release) o Novartis will manufacture CureVac’s vaccine. (press release) o GlaxoSmithKline plc and CureVac N.V. announced a new €150m collaboration, building on their existing relationship, to jointly develop next generation mRNA vaccines for COVID-19 with the potential for a multi-valent approach to address multiple emerging variants in one vaccine. (press release) o Rentschler Biopharma SE will manufacture CureVac’s vaccine. (press release) o Bayer will support the further development, supply and key territory operations of CureVac’s vaccine candidate. (press release) o Fareva will dedicate a manufacturing plant in France to the fill and finish of CureVac’s vaccine. (press release) o Wacker Chemie AG will manufacture CureVac’s vaccine candidate at its Amsterdam site. (press release) o CureVac will collaborate with Tesla Grohmann Automation to develop an RNA printer that works like a mini-factory and can produce such drugs automatically. (press release) • Moderna o Samsung Biologics will provide large scale, commercial fill-finish manufacturing for Moderna’s vaccine in South Korea. (press release) o Baxter International will provide fill/finish services and supply packaging for Moderna. (press release) o Sanofi will manufacture 200 million doses of Moderna’s COVID-19 vaccine starting in September 2021. (press release) o Rovi will produce bulk substance for Moderna’s COVID-19 vaccine, expanding an agreement between the companies. -
Third Quarter 2020
March 31, 2020 Third Quarter 2020 Corporate update and financial results November 10, 2020 Forward-looking statements Various statements in this slide presentation concerning the future expectations of BioNTech, its plans and prospects, including the Company's views with respect to the potential for mRNA and other pipeline therapeutics; BioNTech's efforts to combat COVID-19; the collaborations between BioNTech and Pfizer and Fosun to develop a potential COVID-19 vaccine; our expectations regarding the potential characteristics of BNT162b2 in our continuing Phase 2/3 trial and/or in commercial use based on data observations to date; the expected timepoint for additional readouts on efficacy data of BNT162b2 in our Phase 2/3 trial; the nature of the clinical data for BNT162, BNT311 and our other product candidates, which is subject to ongoing peer review, regulatory review and market interpretation; the timing for submission of data for, or receipt of, any potential approval or Emergency Use Authorization with respect to our BNT162 program; the timing for submission of BNT162 manufacturing data to the FDA; the ability of BioNTech to supply the quantities of BNT162 to support clinical development and, if approved, market demand, including our production estimates for 2020 and 2021 and orders received to-date; the planned next steps in BioNTech's pipeline programs and specifically including, but not limited to, statements regarding plans to initiate clinical trials of BioNTech's product candidates and expectations for data announcements with -
Curevac Announces Financial Results for the Second Quarter and First Half of 2021 and Provides Business Update
CureVac Announces Financial Results for the Second Quarter and First Half of 2021 and Provides Business Update Continuation of corporate transformation into commercial-ready biopharma company o Management team strengthened with appointments of Chief Operating Officer Malte Greune and Chief Development Officer Klaus Edvardsen First-generation COVID-19 vaccine candidate, CVnCoV o Final analysis reported of pivotal Phase 2b/3 study conducted in ten countries in variant-dominated environment o Committed to seeking regulatory approval with EMA – submission of comprehensive clinical data packages within rolling submission ongoing Second-generation COVID-19 vaccine candidate, CV2CoV, jointly advanced with GSK o Preclinical study provides evidence for strongly improved immune responses with second-generation mRNA backbone compared to first-generation backbone during challenge study and against range of variants, including Delta and Lambda variant o Start of CV2CoV Phase 1 clinical trial anticipated in Q4 2021 Oncology Programs o Phase 1 trial extension of lead asset, CV8102, on track to fully recruit o Legacy program, BI 1361849, developed in partnership with Boehringer Ingelheim, based on early protamine formulation terminated; companies assessing options for further collaboration Financials: Cash position of €1.36 billion as of June 30, 2021 TÜBINGEN, Germany/ BOSTON, USA – August 16, 2021 – CureVac N.V. (Nasdaq: CVAC), a global biopharmaceutical company developing a new class of transformative medicines based on messenger ribonucleic acid (“mRNA”), today announced financial results for the second quarter and first half of 2021 and provided business update. “Large parts of the world are still under-vaccinated against SARS-CoV-2, making effective vaccines necessary to prevent further evolution of the virus and to avoid renewed restrictions on public life,” said Franz-Werner Haas, Chief Executive Officer of CureVac. -
J&J Provides Early Hope for Single-Dose Covid-19 Vaccine
January 14, 2021 J&J provides early hope for single-dose Covid-19 vaccine Madeleine Armstrong Pivotal data for JNJ-78436735 are imminent, with Novavax and Curevac not far behind. One advantage of Johnson & Johnson’s Covid-19 vaccine candidate is that it might provide protection after a single dose. Early neutralising antibody data suggest that this might indeed be the case – but, as ever, this needs to be confirmed with efficacy data. Luckily, that is coming very soon: results from the Ensemble trial, testing one dose of JNJ-78436735, are due in late January. Other projects from Novavax and Curevac are also set to yield pivotal data in the first quarter, so it might soon become clear whether more vaccines will be joining the currently authorised options. Selected upcoming readouts with Covid-19 vaccines Vaccine Company Trial name/details N Trial ID Timing name Ensemble, US ph3, single 45,000 NCT04505722 Data due Jan 2021 Johnson & JNJ- dose Johnson 78436735 Ensemble-2, US ph3, two 30,000 NCT04614948 Began Nov 2020 doses Data due early Q1 S Africa ph2b 4,400 NCT04533399 2021 NVX- Data due early Q1 Novavax UK ph3 15,000 NCT04583995 CoV2373 2021 Interim data due Q2 Prevent-19, US/Mexico ph3 30,000 NCT04611802 2021 Herald, Europe ph2/3 36,500 NCT04652102 Data due Q1 2021 CVnCoV Curevac Europe ph3, healthcare Primary completion 2,500 NCT04674189 workers Jun 2021 Primary completion Astrazeneca AZD1222* US ph3 30,000 NCT04516746 Mar 2021 *Authorised in the UK in Dec 2020. Source: EvaluatePharma & clinicaltrials.gov. The latest data came from a phase I/II trial of JNJ-78436735, and were published in the NEJM yesterday; these are updated results from a preprint released in September. -
FDA Covid-19 Response at a Glance Summary As of July 19, 2021
FDA COVID-19 Response At-A-Glance Summary as of July 19, 2021 The U.S. Food and Drug Administration, along with other federal, state, and local agencies and public health officials across the country, continues critical work to protect public health during the pandemic of COVID-19. Major focus areas of the FDA’s response include increasing the availability of tests, therapeutics, vaccines and devices such as ventilators and personal protective equipment, and many other important items necessary for the response. The FDA is also monitoring the human and animal food supply and taking swift action on fraudulent COVID-19 products. Highlights of FDA Activities Ensuring Timely Availability to Accurate • The agency has issued EUAs and policies to help increase and Reliable Tests the availability of personal protective equipment, such as • As of July 16, 396 tests and sample collection devices respirators, gowns, surgical masks, and more. are authorized by the FDA under Emergency Use • There are now more than 630 drug development Authorizations (EUAs); these include 281 molecular programs in planning stages and 11 EUAs for tests and sample collection devices, 85 antibody COVID-19 treatments are currently authorized for and other immune response tests and 30 antigen emergency use. One treatment is currently approved by tests. There are 52 molecular authorizations and one the FDA for use in COVID-19. antibody authorization that can be used with home- collected samples. There is one molecular prescription Facilitating the Development of at-home test, three antigen prescription at-home tests, COVID-19 Vaccines five antigen over-the-counter (OTC) at-home tests, and • There are three COVID-19 vaccines authorized for two molecular OTC at-home tests. -
Investor Presentation
Participants Company overview Pharmaceuticals Oncology Financial review Conclusion Appendix References Q1 2021 Results Investor presentation 1 Investor Relations │ Q1 2021 Results Participants Company overview Pharmaceuticals Oncology Financial review Conclusion Appendix References Disclaimer This presentation contains forward-looking statements within the meaning of the United States Private Securities Litigation Reform Act of 1995, that can generally be identified by words such as “potential,” “expected,” “will,” “planned,” “pipeline,” “outlook,” or similar expressions, or by express or implied discussions regarding potential new products, potential new indications for existing products, potential product launches, or regarding potential future revenues from any such products; or regarding the impact of the COVID-19 pandemic on certain therapeutic areas including dermatology, ophthalmology, our breast cancer portfolio, some newly launched brands and the Sandoz retail and anti-infectives business, and on drug development operations; or regarding potential future, pending or announced transactions; regarding potential future sales or earnings of the Group or any of its divisions; or by discussions of strategy, plans, expectations or intentions; or regarding the Group’s liquidity or cash flow positions and its ability to meet its ongoing financial obligations and operational needs; or regarding our collaboration with Molecular Partners to develop, manufacture and commercialize potential medicines for the prevention and treatment of COVID- 19 and our joining of the industry-wide efforts to meet global demand for COVID-19 vaccines and therapeutics by leveraging our manufacturing capacity and capabilities to support the production of the Pfizer-BioNTech vaccine and to manufacture the mRNA and bulk drug product for the vaccine candidate CVnCoV from CureVac. -
COVID-19 Mrna Pfizer- Biontech Vaccine Analysis Print
COVID-19 mRNA Pfizer- BioNTech Vaccine Analysis Print All UK spontaneous reports received between 9/12/20 and 22/09/21 for mRNA Pfizer/BioNTech vaccine. A report of a suspected ADR to the Yellow Card scheme does not necessarily mean that it was caused by the vaccine, only that the reporter has a suspicion it may have. Underlying or previously undiagnosed illness unrelated to vaccination can also be factors in such reports. The relative number and nature of reports should therefore not be used to compare the safety of the different vaccines. All reports are kept under continual review in order to identify possible new risks. Report Run Date: 24-Sep-2021, Page 1 Case Series Drug Analysis Print Name: COVID-19 mRNA Pfizer- BioNTech vaccine analysis print Report Run Date: 24-Sep-2021 Data Lock Date: 22-Sep-2021 18:30:09 MedDRA Version: MedDRA 24.0 Reaction Name Total Fatal Blood disorders Anaemia deficiencies Anaemia folate deficiency 1 0 Anaemia vitamin B12 deficiency 2 0 Deficiency anaemia 1 0 Iron deficiency anaemia 6 0 Anaemias NEC Anaemia 97 0 Anaemia macrocytic 1 0 Anaemia megaloblastic 1 0 Autoimmune anaemia 2 0 Blood loss anaemia 1 0 Microcytic anaemia 1 0 Anaemias haemolytic NEC Coombs negative haemolytic anaemia 1 0 Haemolytic anaemia 6 0 Anaemias haemolytic immune Autoimmune haemolytic anaemia 9 0 Anaemias haemolytic mechanical factor Microangiopathic haemolytic anaemia 1 0 Bleeding tendencies Haemorrhagic diathesis 1 0 Increased tendency to bruise 35 0 Spontaneous haematoma 2 0 Coagulation factor deficiencies Acquired haemophilia -
Statements Contained in This Release As the Result of New Information Or Future Events Or Developments
Pfizer and BioNTech Provide Update on Booster Program in Light of the Delta-Variant NEW YORK and MAINZ, GERMANY, July 8, 2021 — As part of Pfizer’s and BioNTech’s continued efforts to stay ahead of the virus causing COVID-19 and circulating mutations, the companies are providing an update on their comprehensive booster strategy. Pfizer and BioNTech have seen encouraging data in the ongoing booster trial of a third dose of the current BNT162b2 vaccine. Initial data from the study demonstrate that a booster dose given 6 months after the second dose has a consistent tolerability profile while eliciting high neutralization titers against the wild type and the Beta variant, which are 5 to 10 times higher than after two primary doses. The companies expect to publish more definitive data soon as well as in a peer-reviewed journal and plan to submit the data to the FDA, EMA and other regulatory authorities in the coming weeks. In addition, data from a recent Nature paper demonstrate that immune sera obtained shortly after dose 2 of the primary two dose series of BNT162b2 have strong neutralization titers against the Delta variant (B.1.617.2 lineage) in laboratory tests. The companies anticipate that a third dose will boost those antibody titers even higher, similar to how the third dose performs for the Beta variant (B.1.351). Pfizer and BioNTech are conducting preclinical and clinical tests to confirm this hypothesis. While Pfizer and BioNTech believe a third dose of BNT162b2 has the potential to preserve the highest levels of protective efficacy against all currently known variants including Delta, the companies are remaining vigilant and are developing an updated version of the Pfizer-BioNTech COVID-19 vaccine that targets the full spike protein of the Delta variant. -
Version 12.0, 01 Jun 2018 ANNEX I SUMMARY of PRODUCT
BioThrax® (Anthrax Vaccine Adsorbed) 1.3.1 Summary of Product Characteristics, Labelling and Package Leaflet Version 12.0, 01 Jun 2018 ANNEX I SUMMARY OF PRODUCT CHARACTERISTICS, LABELLING AND PACKAGE LEAFLET Emergent BioSolutions, Inc. Confidential and Proprietary Page 1 of 25 BioThrax® (Anthrax Vaccine Adsorbed) 1.3.1 Summary of Product Characteristics, Labelling and Package Leaflet SUMMARY OF PRODUCT CHARACTERISTICS Emergent BioSolutions, Inc. Confidential and Proprietary Page 2 of 25 BioThrax® (Anthrax Vaccine Adsorbed) 1.3.1 Summary of Product Characteristics, Labelling and Package Leaflet This medicinal product is subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse reactions. See Section 4.8 for how to report adverse reactions 1 NAME OF THE MEDICINAL PRODUCT BioThrax1 suspension for injection. Anthrax Vaccine Adsorbed (purified cell-free filtrate) 2 QUALITATIVE AND QUANTITATIVE COMPOSITION One dose (0.5 mL) contains: Anthrax antigen filtrate: 50 micrograms (50 mcg) a, b For a full list of excipients, see Section 6.1. a Produced from cell-free filtrates of an avirulent strain of Bacillus anthracis b Adsorbed on aluminium hydroxide, hydrated (0.6 mg Al3+) 3 PHARMACEUTICAL FORM Suspension for injection. Sterile, milky-white liquid suspension, when mixed. 4 CLINICAL PARTICULARS 4.1 Therapeutic indications BioThrax is indicated for the prevention of disease caused by Bacillus anthracis, in adults at risk of exposure. BioThrax should be used in accordance with official recommendations, where available. 4.2 Posology and method of administration Posology: Primary Immunisation: 3-doses each of 0.5 mL, given at 0, 1 and 6 months. -
Pfizer-Biontech COVID-19 Vaccine Consent and Screening Form For
Page 1 of 2 Pfizer-BioNTech COVID-19 Vaccine and COMIRNATY (COVID-19 VACCINE, mRNA) Consent and Screening Form for Individuals Under 18 Years of Age SECTION 1: INFORMATION ABOUT MINOR CHILD TO RECEIVE VACCINE (PLEASE PRINT) MINOR’S NAME (Last) (First) (M.I.) MINOR’S DATE OF BIRTH (MM/DD/YEAR): MINOR’S RACE ETHNICITY Is Minor a person White Black Asian Native American or Alaska Native Hispanic with a disability? Native Hawaiian or Pacific Islander Non-Hispanic YES NO PARENT/LEGAL GUARDIAN’S NAME (First) (M.I.) MINOR’S AGE: MINOR’S (Last) GENDER: M / F ADDRESS PARENT/GUARDIAN DAYTIME PHONE NUMBER AND MOBILE NUMBER: CITY STATE ZIP PARENT/GUARDIAN EMAIL ADDRESS: SECTION 2: SCREENING FOR VACCINE ELIGIBILITY The following questions will help determine if there is any reason your child should not get the COVID-19 vaccine. If you answer “yes” to any question, it does not necessarily mean that your child should not be vaccinated. It just means additional questions may be asked. If a question is not clear, please ask your healthcare provider to explain it. YES NO UNKNOWN 1. Is your child currently feeling sick or ill? 2. Has your child ever received a dose of the COVID-19 vaccine? If yes, which vaccine? Moderna; Pfizer; Janssen (Johnson & Johnson); Comirnaty; another brand of vaccine: _________________ Date: ___________ 3. Has your child ever had an allergic reaction to: (This would include a severe allergic reaction [e.g., anaphylaxis] that required treatment with epinephrine or EpiPen® or that caused you to go to the hospital. It would also include an allergic reaction that caused hives, swelling, or respiratory distress, including wheezing.) A component of a COVID-19 vaccine, including any of the following: o Polyethylene glycol (PEG), which is found in some medications, such as laxatives and preparations for colonoscopy procedures? o Polysorbate, which is found in some vaccines, film coated tablets, and intravenous steroids? A previous dose of COVID-19 vaccine? 4. -
Biontech Publishes Data on Novel Mrna Vaccine Approach to Treat Autoimmune Diseases in Science
BioNTech Publishes Data on Novel mRNA Vaccine Approach to Treat Autoimmune Diseases in Science January 7, 2021 Collaborative study of BioNTech with TRON and the University Medical Center and Research Center for Immunotherapy at Johannes Gutenberg University of Mainz introduces novel non-inflammatory mRNA vaccine encoding disease-related autoantigens that suppressed disease activity in several complex mouse models of multiple sclerosis Approach addresses key pitfalls in the treatment of autoimmune diseases such as the induction of systemic immune suppression Approach can easily be tailored to individual disease-causing antigens of patients and confers bystander tolerance to address highly complex, polyclonal and rare autoimmune disease types Represents the first application of BioNTech’s mRNA technology for the purpose of antigen-specific immune-modulation of autoimmune diseases, which further expands BioNTech’s diversified immunology pipeline into another category of disease relevant targets MAINZ, GERMANY, January 7, 2021 (GLOBE NEWSWIRE) —BioNTech SE (Nasdaq: BNTX, “BioNTech” or “the Company”) announced today the publication of preclinical data on its novel mRNA vaccine approach against autoimmune diseases in the peer-reviewed journal Science. The publication titled “A non-inflammatory mRNA vaccine for treatment of experimental autoimmune encephalomyelitis” summarizes the findings on the disease-suppressing effects of a non-inflammatory, nucleoside-modified mRNA vaccine in several clinically relevant mouse models of multiple sclerosis (MS). Autoimmune diseases like MS represent conditions in which the immune system malfunctions and attacks healthy tissue or cells of the body. In MS, the inflammation causes the destruction of the protective myelin sheath that covers the nerve fibers. This damage disrupts the ability to transmit signals between nerve cells and the target tissue resulting in a range of neurological, sensory and motor symptoms that may differ greatly between individuals. -
Report from Accountable.US
NEW ANALYSIS REVEALS $250M IN INSIDER PROFITEERING AT GOVERNMENT-BACKED DRUG COMPANIES, INCLUDING $105M IN NEW TRADES IN LESS THAN 3 MONTHS’ TIME In Six Months Since Launch Of Operation Warp Speed, Execs At Five Drug Companies Made Net Profit Of More Than $250 Million Dumping Their Companies’ Stocks. An earlier report from Accountable.US compiled executive trading data from the launch of Operation Warp Speed on May 15 through August 31, 2020 and found they made stock transactions valued at a net profit of more than $145 million. New analysis of insider transactions at those companies over the six months between May 15 and November 15, 2020, show more than $250 million in net profit. Company Net Profit Emergent BioSolutions $23,906,515.14 Johnson & Johnson $4,276,630.00 Moderna $165,889,439.69 Novavax $46,372,082.90 Pfizer $10,490,165.85 Total $250,934,833.57 From September To Mid-November, Execs At Four Drug Companies Involved In Operation Warp Speed Have Made Net Profit Of More Than $105M Dumping Their Companies’ Stock. According to SEC filings, from the beginning of September through November 15, 2020, executives and directors at four of the companies receiving COVID vaccine funding through Operation Warp Speed have made stock transactions valued at a net profit of more than $105 million. NOTE: Johnson & Johnson did not report any new individual insider transactions during this period. Company Net Profit Emergent BioSolutions $18,860,527.37 Moderna $50,406,146.77 Novavax $29,037,668.05 Pfizer $7,388,569.80 Total $105,692,911.99 • The net profit of these transactions from May 15-November 15, 2020 was $250.9 million; the total profit of these trades was $292.1 million.