A cure for COVID19?
With the governor of Lagos and the comissioner for health at the Landmark COVID19 ISOLATION CENTRE

A cure for COVID19?

I am writing this article as there has been so much noise/confusion about potential cures and remedies. Particularly the syrup from Madagascar. Its written in a very humorous style because its on a very mind-numbingly boring subject: drug discovery.

This is the process of drug discovery and some of the things to think about when you are considering whether something is a cure, a remedy or a feel good drink like Lucozade or Red bull.

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  1. Lab Research

When a substance is suspected to be a cure for a certain disease, 'bench research' or lab research is carried out. This is the R&D phase in a lab with cells in a dish. It is painstaking work.

When I was awarded the MEXT Scholarship to study stem cells in Japan this is what I was doing. Walking from Tokyo Eki to Shimbashi everyday (because no money for transport), resuming at the lab, putting on my white coat.

Drinking green tea, performing experiments on cells, recording my findings, presenting my findings & hoping that we would receive approval to move to pre-clinical phase

Getting approval means you need evidence at the bench stage that this cure worked in your petri dish. Lots of paper work, late nights, presentations at international conferences, weight loss and nerves.Most don't get approval.

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2. Pre-clinical stage

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When you get to the preclinical stage, you are in the game. Then you get to test your cure first on small mammals like mice, then on larger animals.

These animals cannot get sick, these animals need to be monitored, if single thing goes wrong with any animal whether its your drug that caused it or not, these committees don't think like that o.

They are looking for issues/problems/inaccuracies/inconsistencies and they are meticulous!

Any tiny problem. Your research will end, your funding will be cut and you are back to square one. One of the words used in the lab a lot was 'Mendokusai'. In Nigerian slang it would translate to 'long thing'

Research is bothersome, you need attention to detail. And it’s thankless.

So after the bench research that lasts years, the pre-clinical trials (NONE of those mice can die o. Nothing can happen to them.), you seek approval to move to the clinical trial stage. The chances of this are literally one in a million.

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3. Clinical Stage

When you reach clinical trial stage, that is another set of issues. You have to design and execute a randomised, multi-centre, double blind controlled trial.

Meaning you have to test the drug on lots of randomly selected volunteers, in different centres or cities and measure its effectiveness against a fake drug 'placebo'.

The nurses that are giving the drug CANNOT know which drug is real and which is placebo to prevent bias. The patient cannot know if they are getting the real drug of placebo.

That is double blind.

You are paying for hotel, you are paying for the drug, you have not made one penny yet.

You are paying statistician. Don't forget all those mice you paid for in the lab a few years ago.

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At this stage, you may be several hundred million dollars in. And unlike Davido, there is no assurance.

And you don't have 30 billion for akant. You have 30bn potentially down the drain.

There are all sorts of random reasons that you clinical trial may fail, it has to be reviewed by other smart researchers that tear your methods apart. You have to be super careful.

After than, you go for approval. You need a team of like 50 people working at this for months to put all the documents together. This is the FDA and they do not play. They are paid to see problems in all you have done so far.

Many drugs go through this whole process and don't get FDA approval. Because the FDA don't care about the billions that have been spent, or your dreams or you family members that you took money from, or your investors.

They are focused on safety. If your documents don't satisfy them, they won't approve your drug. And they won't feel any remorse.

There is no shortcut. They cannot be bribed. They cannot be hoodwinked. They cannot be blindsided (not usually). This is one of Americas 'strong institutions'

After FDA approval you can start marketing your drug. But then comes the yellow card system.

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All adverse drug reactions across the world need to be reported via this yellow card system to ascertain that if there are any problems in the wider population.

Guess what?? AFTER ALL THAT SUFFERING. Your drug can be withdrawn if a side effect that didn't show up in clinical trials shows up in the wider population. This happened quite famously with COX-2 inhibitors.

COX2 inhibitors were supposed to be the 'miracle drug',I cannot explain all the excitement in the medical world about this drug. All the advantages of a normal NSAID like Ibruprofen, without having the side effect of ulceration.

It went through all the normal process and received approval. And it worked. However, post approval, remember all the work that goes into approval, it was found to cause increased numbers of heart attacks and strokes.

That didn't really show up well in the clinical trials.

Therefore most of them had to be taken off the market.

It was so sad.

Patients that had been in pain for years, were finally painfree. They were going to church to testify about this drug because IT WORKED.

It killed pain, but unfortunately with the side effect of killing people as well.

The biggest scam is people telling you because something is 'natural' it has no side effects or can't kill you. All of these poisonous mushrooms are natural.

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The processes are being relaxed because of COVID19, but there still has to be a process beyond mixing something in your kitchen, announcing it to the press as a cure then asking influencers to trend it.

It's not Brazilian hair.

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Things to look for in any info claiming to be new #COVID19 research/cure

1. CT/MRI/XR results so everyone can see? Blood tests?

2. Proper case series

3. Appropriate number of patients

4. Reported in a Tier 1 journal

5. Peer reviewed

6. Double blind clinical trial

7. Randomized clinical trial

8. Multi-centre clinical trial

9. Who sponsored the research?

10. Statistical significance, Number needed to treat

Gaius Bala

Medical Laboratory Scientist👨🏿🔬| Graduate student; Masters in Molecular Medicine 🧬| Teen coach| Lover of Arts and Literature | Transforming Lives into Nations

4y

Thanks for this!!!!

When economics partner with medicine....We get the best results.. your articles are so educative... Thanks doc ...

Kayode Ijagbemi

Data Science|| Cloud Engineering|| Operational Excellence|| Research

4y

This is a really nice article and it's easy to understand. I sincerely think Madagascar needs to avail their herbal Covid-19 remedy for clinical testing. Obviously from the results they've been getting, it deserves a shot but it could be a situation of saving the present to destroy the future as its adverse effects ain't known.

Uju Paulcy

𝐅𝐨𝐮𝐧𝐝𝐞𝐫 & 𝐆𝐫𝐨𝐮𝐩 𝐂𝐡𝐢𝐞𝐟 𝐄𝐱𝐞𝐜𝐮𝐭𝐢𝐯𝐞 𝐚𝐭 𝐈𝐍𝐕𝐄𝐓𝐀 𝐆𝐑𝐎𝐔𝐏 African Economic Envoy |Grand Scale Project Financier| International & Intra Africa Trade Facilitator |TV Host: Invest & Trade Africa

4y

Very Insightful Ola Brown. I am thinking if all the myraids of drugs I see everywhere went through this approval. Possibly there are different regional structures to this measures like you mentioned the FDA. Or does the FDA regulate all drugs in the world except those sold in America? My goal is does Africa have a process testing methods for drugs in her region; And what if the covid Organics produced by Madagascar was made into tea using the artemisia plant and there was a possibility that it could work on covid or prevent it. Does it require such humongous details to get to the market?

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