vaccine phase 3 success rate
Potential Pricing: AstraZeneca has said that it would make the vaccine available globally on a non-profit basis, through the course of the current pandemic. Media Relations These trials will determine if the vaccine protects against Covid-19 and whether it will be cleared for use in the general public. In addition, the companies announced that the safety milestone required by the U.S. Food and Drug Administration (FDA) for Emergency Use Authorization (EUA) has been achieved. [8] Moderna also provided an update on its phase 2 trials which are currently underway, noting that it had enrolled 350 out of its total planned 600 participants for the study. Oncology drugs have a puny 3.4% success rate, while vaccines for infectious diseases have a … Did you know that the U.S. government awarded biotech company Novavax $1.6 billion toward the development of its Covid-19 vaccine? Based on its deep expertise in mRNA vaccine development and in-house manufacturing capabilities, BioNTech and its collaborators are developing multiple mRNA vaccine candidates for a range of infectious diseases alongside its diverse oncology pipeline. PubMed PMID: 22843783. external icon Moderna (NASDAQ: MRNA) stock has jumped by almost 40% over the last two days (including after-hours trading Tuesday), driven by two positive developments. On the other hand, big pharma companies such as Johnson & Johnson (up 5% year to date) and Sanofi (down 4%), who remain in the pre-clinical stage, could offer better downside protection, given their highly diversified revenue streams. We strive to set the standard for quality, safety and value in the discovery, development and manufacture of health care products, including innovative medicines and vaccines. In order to compute the probability of a vaccine development program making it all the way from phase 1 to approval, we consider only the vaccine development programs that have definite outcomes. Topline data on the AstraZeneca vaccine from a Phase 3 trial were released in November.Tuesday’s results — the first Phase 3 clinical data for a Covid vaccine … Data on whether the candidate vaccines protect against illness, and for how long, won’t come until large Phase 3 trials, slated to start as soon as this month, begin returning results this fall. Pfizer’s vast resources, better access to manufacturing, and distribution could give it an edge over Moderna as it continues to move forward. The Phase 3 vaccine efficacy trial, known as COVE, was begun under OWS, a multi-agency collaboration led by HHS and the Department of Defense that aims to accelerate the development, manufacturing and distribution of medical countermeasures for COVID-19. Pfizer shares traded 9% higher to a new 52-week high price after the company reported that interim data from its Phase 3 COVID-19 vaccine trial with BioNTech showed a 90% success rate in participants without prior evidence of SARS-CoV-2 infection. 2014 Feb;58(3):319-27. doi: 10.1093/cid/cit736. The platform uses extensive data to show in a single snapshot what drives the value of a company's business. [5], German biotech company BioNTech is working on a Covid-19 vaccine in partnership with Pfizer (NYSE: PFE). Overall, the two companies appear to be roughly at the same stages in the clinical timeline. Overall, the pharma industry is moving much faster than expected with Covid-19 vaccine development. Moderna (NASDAQ: MRNA) has outlined plans for phase 3 clinical trials for its Covid-19 vaccine candidate mRNA-1273, which will begin in July and is expected to include about 30,000 participants. Phase 1 trials usually involve a few dozen people and are designed to observe whether a vaccine or drug is safe. Can Editas Medicine Stock Bounce Back After A 13% Drop In 5 Days ? Pfizer Inc. (NYSE: PFE) and BioNTech SE (Nasdaq: BNTX) today announced that, after conducting the final efficacy analysis in their ongoing Phase 3 study, their mRNA-based COVID-19 vaccine candidate, BNT162b2, met all of the study’s primary efficacy endpoints. Based on current projections, the companies expect to produce globally up to 50 million vaccine doses in 2020 and up to 1.3 billion doses by the end of 2021. News18 » News » India » From Vaccine Candidates to Success Rates, All You Wanted to Know About Covid-19 Shot Trials in India. (Photo Illustration by Jakub Porzycki/NurPhoto via Getty Images), America's Top Givers: The 25 Most Philanthropic Billionaires, EY & Citi On The Importance Of Resilience And Innovation, Impact 50: Investors Seeking Profit — And Pushing For Change. NEW YORK & MAINZ, Germany--(BUSINESS WIRE)-- Consistent with our responsibility as one of the world's premier innovative biopharmaceutical companies, we collaborate with health care providers, governments and local communities to support and expand access to reliable, affordable health care around the world. The company is expected to receive as much as $483 million in U.S. federal government funding for its vaccine development. +1 (212) 733-7410 The company intends to enroll a total of 600 participants in the study, up from 45 participants in the phase 1 study. Analysis of the data indicates a vaccine efficacy rate of 95% (p<0.0001) in participants without prior SARS-CoV-2 infection (first primary objective) and also in participants with and without prior SARS-CoV-2 infection (second primary objective), in each case measured from 7 days after the second dose. This press release features multimedia. About Pfizer: Breakthroughs That Change Patients’ Lives. The Gamaleya Center. In comparison, Johnson and Johnson and Pfizer are down year-t0-date. "Today is a great day for science and humanity. There are a couple of developments that could be putting pressure on the stock. Clin Infect Dis. While the development uses messenger RNA technology similar to Moderna, this effort focuses on not just one, but four prototypes. Repeating the logic for the transitions between phase 2 and phase 3, and between phase 3 and approval, gives 65.4% and 80.1% as estimates of PoS 23 and PoS 3A, respectively. Early results from trials of a Covid vaccine developed in Russia suggest it could be 92% effective. Based on historical data, the probability of success for a drug moving from phase 1 of clinical trials to phase 2 stands at about 63%, while the metric is sharply lower at 31% for phase 2 to phase 3 progression. Separately, Moderna also said that the federal government has committed $472 million in funding to help the clinical development and production scale-up for its vaccine. TreSecondly, there are some concerns regarding the timeline for the potential approval of Moderna’s vaccine. Find out in our analysis Trefis Theme: Covid-19 Vaccine Portfolio. Is Jabil The Best Stock To Play iPhone 12 Cycle Without Overpaying? A further description of risks and uncertainties can be found in Pfizer’s Annual Report on Form 10-K for the fiscal year ended December 31, 2019 and in its subsequent reports on Form 10-Q, including in the sections thereof captioned “Risk Factors” and “Forward-Looking Information and Factors That May Affect Future Results”, as well as in its subsequent reports on Form 8-K, all of which are filed with the U.S. Securities and Exchange Commission and available at www.sec.gov and www.pfizer.com. Clinical Trial Timeline: Oxford and AstraZeneca have been combining the stages of their clinical trials and are carrying out late-stage phase 2/3 trials in the UK, Brazil, and South Africa. Epub 2012 Jul 25. While Sanofi will contribute the antigen, GSK will provide its pandemic adjuvant technology, which helps to reduce the amount of vaccine protein required per dose. The company has an agreement with the Serum Institute of India, which is the world’s largest vaccine manufacturer. CEO Stephane Bancel recently estimated the probability of success of the vaccine at close to 80% to 90%, citing the effectiveness of the company’s RNA based platform on other viruses such as MERS, Zika, and Cytomegalovirus. +1 (212) 733-3901 Epub 2013 Nov 13. external icon. One of the biggest challenges in estimating the success rate of clinical trials is a… This release contains forward-looking information about Pfizer’s efforts to combat COVID-19, the collaboration between BioNTech and Pfizer to develop a potential COVID-19 vaccine, the BNT162 mRNA vaccine program, and modRNA candidate BNT162b2 (including qualitative assessments of available data, potential benefits, expectations for clinical trials, anticipated timing of regulatory submissions and anticipated manufacturing, distribution and supply), that involves substantial risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements. For more details on the stock price and fundamental performance of some of the key U.S. listed companies developing a coronavirus vaccine, view our COVID Vaccine Portfolio. Good to know, given that the stock is up 3x this year, driven largely by the Coronavirus, meaning that the downside risk could also be considerable. Moderna COVID-19 vaccine candidate mRNA-1273 is now soon going to commence a 30,000-person phase 3 trial in just a matter of six months after it was created Moderna CEO Stephane Bancel claims that his company’s COVID-19 vaccine has an 80 to 90 percent chance of getting FDA approval Moderna’s most complex offering was a vaccine against cytomegalovirus or CMV. This could at least initially limit the pricing power for a potential Moderna vaccine. Efficacy was consistent across age, gender, race and ethnicity demographics. A review of unblinded reactogenicity data from the final analysis which consisted of a randomized subset of at least 8,000 participants 18 years and older in the phase 2/3 study demonstrates that the vaccine was well tolerated, with most solicited adverse events resolving shortly after vaccination. At Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives. Success probabilities do not capture the varied … Moderna (+160% YTD return, $16.8 billion market cap): Moderna was the first to begin phase 1 clinical trials for its RNA-based vaccine. The data is based on 20 cases of Covid-19 from 16,000 volunteers given the Sputnik V vaccine … The trial will continue to collect efficacy and safety data in participants for an additional two years. Pfizer and BioNTech Conclude Phase 3 Study of COVID-19 Vaccine Candidate, Meeting All Primary Efficacy Endpoints, Therapeutic Modalities and Technology Platforms, Small Molecule Product & Process Development, Maintaining Emotional Well-Being During COVID-19, Coronavirus disease (COVID-19) Scientific Resources, Meet our new Chief Patient Officer, Dr. Dara Richardson-Heron, Creating Cures Through Facility Investments, https://www.businesswire.com/news/home/20201118005595/en/. Limitations: The study did not account for preclinical development and relied primarily on ClinicalTrials.gov and FDA resources. Firstly, on Monday, the Nasdaq indicated that the Moderna would be included as a component of the Nasdaq-100 index starting from July 20th. Surprisingly, the founders of Trefis discovered that along with most other people they just did not understand even the seemingly familiar companies around them: Apple, Google, Coca Cola, Walmart, GE, Ford, Gap, and others. [Updated 7/6/2020] The Recent Moderna Selloff. Sylke Maas, Ph.D. There were 10 severe cases of COVID-19 observed in the trial, with nine of the cases occurring in the placebo group and one in the BNT162b2 vaccinated group. The probabilities of advancing from phase 1 to 2, phase 2 to 3, and phase 3 to licensure within the total available follow-up time were 38.2% (CI, 30.7% to 45.0%), 38.3% (CI, 23.1% to 50.5%), and 61.1% (CI, 3.7% to 84.3%), respectively. The clinical-stage biotech company has phase 2 trials underway for its vaccine candidate mRNA-1273 and is expected to commence phase 3 trials in July, in collaboration with the U.S. National Institutes of Health. We routinely post information that may be important to investors on our website at www.Pfizer.com. German biotech player BioNTech and Pfizer who are collaborating on a Covid-19 vaccine, released encouraging preliminary early-stage data on their vaccine candidate noting that it was well-tolerated and that it generated significant levels of antibodies in people. Sorry, you need to enable JavaScript to visit this website. Consistent with earlier shared results, older adults tended to report fewer and milder solicited adverse events following vaccination. Pfizer’s vaccine is now roughly in the same stage as Moderna’s in the clinical trial timeline, with the company making plans for Phase 3 trails. Moderna (NASDAQ: MRNA) announced that it has started phase 3 trials of its Covid-19 vaccine candidate mRNA-1273 in collaboration with two U.S. government agencies. While phase 1 trials are used to ascertain the safety of a vaccine or treatment in humans, phase 2 trials gauge the effectiveness and also provide more data on how safe it is. This is in addition to the $483 million in funding it secured from the government in April. The phase 3 trial will help to validate this at a larger scale and is expected to enroll 30,000 participants in the U.S. See our Theme of Covid-19 Vaccine Stocks for an overview of U.S. listed companies working on Covid-19 vaccines and their financial performance and returns. How many people have been vaccinated? View our indicative themes Coronavirus Treatment Stocks, and Coronavirus Testing Stocks for more details on the stock price and fundamental performance of some of the key U.S. listed companies. Trefis is currently used by hundreds of thousands of investors, company employees, and business professionals. American biotech company Moderna has announced on June 11 that will start final stage of covid-19 vaccine trial in July. Pharma bellwether Johnson & Johnson’s vaccine is expected to start phase 1/2a trials over the second half of July. Moderna is looking to start phase 3 trials for the vaccine this month and has indicated that it could have data from the study by Thanksgiving. The FDA said that a Covid-19 vaccine would need to show at least 50% efficacy in a placebo-controlled clinical trial while also spelling out other requirements. Days after Pfizer revealed the first interim Phase 3 … While the company is ahead of larger firms in getting to human trials for its vaccine candidate, it could remain a speculative bet for investors, given its relatively limited revenue streams (just $4 million in revenue over 2019). Separately, there was also a report that Moderna was delaying the start of its Phase 3 trials, although this was denied by the company. While the markets have tumbled due to the spread of the novel coronavirus, stocks of pharma companies developing vaccines and treatments for the highly contagious viral infection have fared well. The Phase 3 clinical trial of BNT162b2 began on July 27 and has enrolled 43,538 participants to date, 38,955 of whom have received a second dose of the vaccine candidate as of November 8, 2020. Every day, Pfizer colleagues work across developed and emerging markets to advance wellness, prevention, treatments and cures that challenge the most feared diseases of our time. Inovio Pharmaceuticals (+255% YTD return, $1.7 billion market cap): Inovio, a small biotech company started phase 1 clinical trial for a DNA-based novel coronavirus vaccine earlier this month. [3] More specifically, after two doses, the vaccine produced neutralizing antibodies - which are key to fighting the virus - that were 4x higher than what was found in patients who had recovered from coronavirus infections. For perspective, each phase of a vaccine development typically takes multiple years and per a 2013 study, the total development time for the average vaccine was close to 11 years. Phase 1 trials usually involve a few dozen people and are designed to observe whether a vaccine or drug is safe. (Photo Illustration by Jakub Porzycki/NurPhoto via Getty Images), [Updated 7/29/2020] Moderna Begins Phase 3 Trials. While Moderna was seen as one of the leaders in the vaccine race, rivals are also catching up quickly. Phase 1, 2, and 3 trials: Clinical trials typically take place in three stages. This would be a real concern for Moderna investors, who have bid the stock up 4x this year, in anticipation of potential profits from the vaccine candidate. This puts Moderna well ahead of rivals in the clinical trial timeline - rival biotech Inovio’s candidate is in phase 1, while many other U.S. based players remain in the pre-clinical phase. Sanofi (-4% YTD return, $120 billion market cap): Sanofi has joined forces with GlaxoSmithKline to develop a coronavirus vaccine. This information—including product information—is intended only for residents of the United States. See all Trefis Price Estimates and Download Trefis Data here, What’s behind Trefis? Does this make Novavax a better bet that Moderna? Which stocks offer a better risk to reward profile? +49 (0)6131 9084 1074 As shown, the overall probability of success for all drugs and vaccines is 13.8%. Medical syringe is seen with Moderna company logo displayed on a screen in the background in this ... [+] illustration photo taken in Poland on June 12, 2020. At this rate, the company could be on track to win full approval for the vaccine by next year. Moderna says that it could begin phase 2 trials as early as Spring 2020, with phase 3 trials potentially starting as early as the Fall. In the Phase 3 trial, the vaccine was generally well tolerated, with adverse reactions similar to those of other childhood vaccines. But this number masks a wide variation by therapeutic area. These forward-looking statements may include, but may not be limited to, statements concerning: BioNTech’s efforts to combat COVID-19; the collaboration between BioNTech and Pfizer to develop a potential COVID-19 vaccine; our expectations regarding the potential characteristics of BNT162b2 in our 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, which is subject to ongoing peer review, regulatory review and market interpretation; the timing for submission of data for, or receipt of, any potential Emergency Use Authorization; the timing for submission of manufacturing data to the FDA; and 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. Although vaccine bets still remain quite speculative, considering that most companies are either in the pre-clinical or phase 1 stage of trials for their candidates, companies could see significant upside if they develop a safe, effective, and relatively affordable vaccine. For phase 3 to the new drug application - a stage just before approval - the POS stands at 58%. Moderna has also announced a collaboration with Switzerland based Lonza Group for manufacturing its vaccine, producing as much as 1 billion doses each year. Russian researchers suggest their vaccine is both safe and 92 percent effective at protecting against COVID-19. Should you pick Johnson & Johnson Or Pfizer For Better Returns? Phase 1, 2, and 3 trials: Clinical trials typically take place in three stages. The company has partners to manufacture and distribute about 2 billion doses of its experimental Covid-19 vaccine. These data also will be submitted to other regulatory agencies around the world. “The study results mark an important step in this historic eight-month journey to bring forward a vaccine capable of helping to end this devastating pandemic. [Updated 6/12/2020] What To Expect As Moderna Plans Phase 3 Trials. [7]. They can be used be as temporary storage units for 15 days by refilling with dry ice. Recent data show increasing rates of severe ... authorization. Approximately 42% of global participants and 30% of U.S. participants have racially and ethnically diverse backgrounds, and 41% of global and 45% of U.S. participants are 56-85 years of age. On Monday, Oxford University, which is developing a Covid-19 vaccine candidate along with AstraZeneca, published some positive data on phase 1/2 trials, indicating that the vaccine was tolerated and generated a robust immune response. Without up-to-date estimates of the POS, however, investors may misjudge the risk and value of drug development, leading to lost opportunities for both investors and patients. That said, the stock could have significant downside risk as well, as the company does not have any other products in the market, besides a flu vaccine that is in the late stages of development. Prudent resource allocation relies on the accurate and timely assessment of risk. For a discussion of these and other risks and uncertainties, see BioNTech’s Annual Report on Form 20-F filed with the SEC on March 31, 2020, which is available on the SEC’s website at www.sec.gov. [Updated 7/21/2020] Does Oxford-AstraZeneca’s Progress With Covid-19 Vaccine Impact Moderna? Did you know that Johnson & Johnson will begin human trials of its Covid-19 vaccine over the second half of July, well ahead of its previous timeline of September? Media Relations The first primary objective analysis is based on 170 cases of COVID-19, as specified in the study protocol, of which 162 cases of COVID-19 were observed in the placebo group versus 8 cases in the BNT162b2 group. As passive investing is gaining momentum, this could generally increase demand for Moderna stock. This could potentially delay the approval process for Moderna. Johnson & Johnson (+5% YTD return, $390 billion market cap): The pharmaceutical giant could begin phase 1 trials for its coronavirus vaccine by September 2020, at the latest. So how do the Moderna and Oxford-AstraZeneca vaccines’ developments compare? Pharmaceutical manufacturer Johnson & Johnson announced Friday that early trials of a COVID-19 vaccine showed a 98 percent success rate in showing a … The products discussed herein may have different labeling in different countries. The Company exploits a wide array of computational discovery and therapeutic drug platforms for the rapid development of novel biopharmaceuticals. [1] This comes about a week after Moderna released similar progress on its Covid-19 vaccine candidate mRNA-1273. [Updated 7/14/2020] Moderna’s Promising New Data On Phase 1, Inclusion Into Nasdaq Index. The first set of results from our Phase 3 COVID-19 vaccine trial provides the initial evidence of our vaccine’s ability to prevent COVID-19,” said Dr. Albert Bourla, Pfizer Chairman and CEO. Find out more in the Trefis Theme: Coronavirus Vaccine which details key financial, valuation, and returns metrics for the companies. While the stocks of smaller, specialized players such as Inovio Pharmaceuticals and Moderna have rallied by ~250% and ~160% respectively year to date, as both companies already have candidates in Phase 1 trials, these companies also have a much higher risk, given their very limited revenue streams. The company could have a leg up over rivals in terms of production capacity and distribution reach, as it says it would be able to produce as much as 900 million doses by early 2021. This might include you though you may have invested money in these companies, or may have been working with one of them for years as an employee, or have consulted with them as an expert for a long time. The first effective coronavirus vaccine can prevent more than 90% of people from getting Covid-19, a preliminary analysis shows. Moderna said that it commenced stage 2 trials for its new Coronavirus vaccine candidate mRNA-1273 last week. Earlier this week, the FDA provided guidelines for the approval of Covid-19 vaccines, indicating that it would not be relaxing any standards. Volunteer participating in phase 3 trial of the Sinovac COVID-19 vaccine in Padjadjaran University, Bandung, West Java, Indonesia. Four of Pfizer’s facilities are part of the manufacturing and supply chain; St. Louis, MO; Andover, MA; and Kalamazoo, MI in the U.S.; and Puurs in Belgium. [Updated 6/25/2020] Where Do Key Vaccine Efforts Stand Currently? However, the trials should be quicker, as Moderna said it is looking to start phase 3 trials by July. In the U.S., 18.4 million doses administered, with 5.44 million doses in the U.K. and 726,786 in Canada We continue to move at the speed of science to compile all the data collected thus far and share with regulators around the world,” said Dr. Albert Bourla, Pfizer Chairman and CEO. Additionally, the progression from phase 2 to phase 3 may be more tricky for pharma companies. Efficacy and safety: On December 8, The Lancet published an interim analysis of four of Oxford’s phase three trials. For phase 3 to the new drug application - a stage just before approval - the POS stands at 58%. For more information, please visit www.BioNTech.de. The companies have developed specially designed, temperature-controlled thermal shippers utilizing dry ice to maintain temperature conditions of -70°C±10°C. Novavax (440% YTD return, $1.1 billion market cap): Novavax, a company that focuses on vaccines for infectious diseases, has indicated that it has a vaccine candidate called NVX-CoV2373 that has demonstrated effectiveness against the coronavirus in pre-clinical trials. Moderna (NASDAQ: MRNA) stock has declined by close to 10% over the last two trading days. The Phase 3 clinical trial of BNT162b2 began on July 27 and has enrolled 43,661 participants to date, 41,135 of whom have received a second dose of the vaccine candidate as of November 13, 2020. Firstly, the competition could be gaining some ground in the vaccine race. Jasmina Alatovic Copyright © 2002-2021 Pfizer Inc. All rights reserved. I want to thank all the devoted women and men who contributed to this historically unprecedented achievement. While Moderna (NASDAQ: MRNA) was viewed as a front-runner in the race for a Covid-19 vaccine, competition is mounting. The probability of success (POS) of a clinical trial is critical for clinical researchers and biopharma investors to evaluate when making scientific and economic decisions. [email protected], Investor Relations Should You Buy Johnson & Johnson Stock At $160? Pfizer and BioNTech plan to submit a request within days to the FDA for an EUA based on the totality of safety and efficacy data collected to date, as well as manufacturing data relating to the quality and consistency of the vaccine. On Monday, Pfizer and its German partner BioNTech indicated that they also started late-stage trials for their Covid-19 vaccine, which could involve up to 30,000 participants. Any forward-looking statements in this press release are based on BioNTech current expectations and beliefs of future events, and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements. Phase 2 trials may be viewed as more crucial compared to other phases for a couple of reasons. [email protected], BioNTech: Its broad portfolio of oncology product candidates includes individualized and off-the-shelf mRNA-based therapies, innovative chimeric antigen receptor T cells, bi-specific checkpoint immuno-modulators, targeted cancer antibodies and small molecules. The probability of FDA approval after submitting a New Drug Application (NDA) or Biologic License Application (BLA), taking This is significant as most company-sponsored Phase III trials are the longest and most expensive trials to conduct. Moderna (NASDAQ: MRNA) is seen as the front-runner in the race to develop a Covid-19 vaccine. Biopharmaceutical New Technologies is a next generation immunotherapy company pioneering novel therapies for cancer and other serious diseases. “With hundreds of thousands of people around the globe infected every day, we urgently need to get a safe and effective vaccine to the world.”, “We are grateful that the first global trial to reach the final efficacy analysis mark indicates that a high rate of protection against COVID-19 can be achieved very fast after the first 30 µg dose, underscoring the power of BNT162 in providing early protection,” said Ugur Sahin, M.D., CEO and Co-founder of BioNTech. BioNTech’s German sites will also be leveraged for global supply. Based on historical data, the probability of success for a drug … In comparison, Moderna’s collaboration with Swiss biotech company Lonza could enable it to produce as much as one billion doses per year. To date, the Data Monitoring Committee for the study has not reported any serious safety concerns related to the vaccine. [6] There is also a possibility that phase 3 trials could begin as early as July, per the Wall Street Journal. [email protected]. illustration photo taken in Poland on June 12, 2020. Moreover, the company is also working on antiviral treatments against the coronavirus. What does Moderna’s Pipeline Beyond The Covid-19 Vaccine look like? For more than 150 years, we have worked to make a difference for all who rely on us. viability. See How It’s Powering New Collaboration and What-Ifs For CFOs and Finance Teams | Product, R&D, and Marketing Teams, Led by MIT engineers and Wall Street analysts, Trefis (through its dashboards platform dashboards.trefis.com) helps you understand how a company's products, that you. Pfizer is confident in its vast experience, expertise and existing cold-chain infrastructure to distribute the vaccine around the world. (If oncology drugs are excluded, the figure is 20.9%.) A vaccine trial is a clinical trial that aims at establishing the safety and efficacy of a vaccine prior to it being licensed. Pfizer assumes no obligation to update forward-looking statements contained in this release as the result of new information or future events or developments. [9]. BioNTech has established a broad set of relationships with multiple global pharmaceutical collaborators, including Genmab, Sanofi, Bayer Animal Health, Genentech, a member of the Roche Group, Regeneron, Genevant, Fosun Pharma, and Pfizer. Our indicative portfolio of 7 U.S. listed companies developing vaccines for Coronavirus has gained a whopping ~130% year-to-date on an equally weighted basis. 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