Ocugen Investoren 2022 WKN: A2PSZH ISIN: US67577C1053 Forum: Aktien User: Ad_Astra

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Kommentare 6.439
Ad_Astra
Ad_Astra, 08.01.2022 15:05 Uhr
0
Omicron kommt bald
Ad_Astra
Ad_Astra, 08.01.2022 15:04 Uhr
2
COVAXIN Booster Dose 💉💉💉 1⃣3rd dose leads 5X antibodies 🆚 2 dose 2⃣3rd Dose neutralising all variants (Omicron results 🔜) 3⃣Increase in Breadth & Depth of Immune responses 3⃣No safety concerns/favourable risk-benefit profile 4⃣Long term T&B cell responses after 2 doses.
Ad_Astra
Ad_Astra, 08.01.2022 14:33 Uhr
5
Covaxin Booster Dose Safe and Highly Immunogenic (against all variants) #covaxin #BharatBiotech #COVID19Vaccine #COVID19 #boosterdose #SARS_CoV_2
Ad_Astra
Ad_Astra, 08.01.2022 14:32 Uhr
2
https://twitter.com/bharatbiotech/status/1479800788335542273?s=21
Ad_Astra
Ad_Astra, 08.01.2022 14:32 Uhr
1
Booster
Flowy55
Flowy55, 08.01.2022 14:27 Uhr
1
https://twitter.com/BharatBiotech/status/1479800788335542273?s=20
Ad_Astra
Ad_Astra, 08.01.2022 13:51 Uhr
1
https://twitter.com/bharatbiotech/status/1479797790041513984?s=21
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BörsenBuffet, 08.01.2022 12:19 Uhr
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Sean Lee -- Citi -- Analyst My first one is on the supply agreement with Bharat. So does that cover a potential commercial supply, if you're EUA for the pediatric population is approved? How much supply would you have access to and also in terms of the tech transfer to Jubilant? What's the progress on and the expected timeline on that? Shankar Musunuri -- Chairman and Chief Executive Officer Yes, upon EUA, our supply agreement does include adequate doses, Sean, and our partners have significantly increased that capacity this year. And also so that they don't how many restrictions for export. So we will be -- we'll get adequate supply whatever is needed post EUA in the US. And as for as technology transfer is concerned at Jubilant HollisterStier, the program is going well and we are anticipating completion of establishing that including process validations in the first half of next year. So that, we can switch the supply and so the initial part of the supply does include -- even we did see a product from biotech our partners it will include US packaging and the testing from the US release site, which have been established. Sean Lee -- Citi -- Analyst Once the tech transfer is completed next year, would you need additional CMC validation from the FDA to show that the clinical batch and the commercial batch of the same? Shankar Musunuri -- Chairman and Chief Executive Officer Yeah. That's a normal part of the process when you add an additional site, you always have to show the compatibility and that would be the product process.
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BörsenBuffet, 08.01.2022 12:19 Uhr
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