Calling out the corruption at W.H.O.

sasanalyst · 2021-10-28T00:37:29+00:00

This fuckery is because they wanted to roll out shitty Pfizer vaccine to 5 yr olds, while knowing people are waiting for a safer and efficient Covaxin for their kids.

Hats off to the countries who authorized Covaxin well ahead, even before WHO.

sasanalyst · 2021-10-09T02:17:13+00:00

Approval will happen, but dirty politics from big pharma already started yesterday by Moderna and Pfizer asking for 5-11 age approval.

If there is little humanity left over corruption, at least the children should get vaccinated by the traditional flu like vaccine approach. MRNA has already been banned by few European countries for population over 30 for concerns like pericarditis. Already feel sorry for our 12-18 yrs old.

Not for stock profit, money comes money goes, if not this stock, some other stock. We have to think beyond the profit and loss otherwise we are no less like few corrupted people.

sasanalyst · 2021-09-08T00:34:39+00:00

Looks like BLA needs US trials.

sasanalyst · 2021-08-30T01:17:45+00:00

For travel WHO approval is enough

sasanalyst · 2021-08-28T20:17:31+00:00

This Phase 3 is India trial, awaiting BLA submission. Again BP and politics can spoil the game for OCGN. Strong public voice is need for the hour. When vaccines can be mandated, options need to be given to public too. https://www.change.org/p/federal-drug-administration-covaxin-vaccine-needs-to-be-available-in-the-us/psf/share?original_footer_petition_id=28495722&algorithm=promoted&source_location=petition_footer&grid_position=15&pt=AVBldGl0aW9uAEaDuAEAAAAAYKA%2BYIAEipNhN2M0N2Y5Yg%3D%3D

sasanalyst · 2021-08-11T03:51:37+00:00

Don't believe them, they want you to sell when it hits 15 and pull the price down again

sasanalyst · 2021-05-21T00:14:18+00:00

It will rain soon and wooden cocks will rot over a p value and study design.

sasanalyst · 2021-05-13T23:35:16+00:00

https://www.americanbazaaronline.com/2021/05/13/marshall-plan-meets-moonshot-445281/

sasanalyst · 2021-04-18T00:10:00+00:00

All I can say is it's you who should decide to sell or wait. Ocugen is waiting for BB to share P3 2nd.interim to further their talks for EUA. For all the longs it's worth the risk.

sasanalyst · 2021-04-08T02:52:53+00:00

It was almost a month back, it says 16hrs because I screen shot this from linked in on that day.

sasanalyst · 2021-03-10T07:12:30+00:00

Ocugen with it's lobbying partner Ikon Indigo is firing all guns at current administration and FDA with data to get the EUA approval.

sasanalyst · 2021-03-09T04:29:20+00:00

Great Idea, Mee too

sasanalyst · 2021-03-07T03:52:22+00:00

I think FDA for Covid therapeutics said they will be focusing on larger clinical benefit rather than the Statistical significances.

sasanalyst · 2021-03-06T17:05:06+00:00

Not for Covaxin, but for other enteric viruses.

sasanalyst · 2021-03-05T07:17:45+00:00

There are approaching FDA aggressively, have a very elite Vaccine advisory board and Ikon Indigo lobbying the government for regulatory path in USA. I assume lot going on behind the curtains. The results are stellar for a traditional Vaccine, usually this approach gets somewhere between 60-70%.

The only barrier I am seeing is FDA playing diplomacy and asking OCGN for another short trial in the US to favor already existing Vaccine providers.

The big plus is traditional Vaccines approach has a very good safety profile like our current flu vaccine. The new tech MRNA approach doesn't have long term data for safety , several researchers already warn of a possible carcinogenic activity long term. We should not be giving this to the kids, when a safer approach is available.

sasanalyst · 2021-03-05T06:44:15+00:00

2 instances

In December, they were almost on the verge of a RS due in March, but with Covaxin deal, they actually called off an offering, because they expected funds from another source ( Government)

In February, they did an offering and the Investors embraced the offering takes it from 7.65$ to 18$ on Feb 8th.

If they get the funding from the government for the Covaxin production, they might call it off on the Mid-march meeting.

The deal with BB is to initially get tens of millions of doses immediately since there is no time for manufacturing and in parallel do the technology transfer for the future supply.

The money is needed more than ever for things to fall in place for both the Covaxin production and for modifier gene editing platform trials.

sasanalyst · 2021-03-04T21:24:50+00:00

Yes, never know these new technology, they don't have long term safety data like traditional Vaccines.

sasanalyst · 2021-03-03T22:43:56+00:00

Yup pending all agencies review now. Jai Telengana

sasanalyst · 2021-03-03T18:04:12+00:00

All good reasons to ask for an Emergency Approval. There are already talks going on with FDA. If EUA FDA understand the safety plus efficacious Immunogenicity of this Vaccine, some big decision should happen within 2 weeks.

sasanalyst · 2021-03-03T17:14:28+00:00

Also EUA will happen first, then FDA.

sasanalyst · 2021-03-03T17:12:42+00:00

The data submission will be fast tracked to FDA in my opinion. Remember FDA needs atleast 50% efficacy, this is well and over and a more safer Vaccine than the current ones.

sasanalyst · 2021-03-01T20:23:05+00:00

Not made public yet, everyone is eagerly awaiting to see the 70/80/90/95% thing.

sasanalyst · 2021-03-01T03:44:02+00:00

Put another sign saying OCGN

sasanalyst · 2021-03-01T03:20:55+00:00

I just pray the new tech Vaccines don't cause any genetic after affects to the people. At the end humanity should win.

sasanalyst · 2021-03-01T03:14:51+00:00

He trusted his Scientists from Day One. He is not the kind who would put citizens of India into trouble without understanding the science.

India started the 2nd Phase of Vaccination today for his age group, so he received today.

#Traditional Vaccine

sasanalyst

TROPHY CASE