FDA approval is hard to get as these 2 companies are finding out

There are several ASX health companies that are aspiring to sell their medical devices or drugs in the USA. This involves getting the device or drug, or the plans for a clinical trial, approved by the FDA (Food and Drug Administration).

But it is easier said than done as shareholders of Island Pharmaceuticals (ASX:ILA) and Mesoblast (ASX:MSB) have been learning the hard way. 

 

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Island Pharmaceuticals’ plans knocked back by the FDA

(ASX:ILA) is developing a drug it hopes can fight mosquito diseases, particularly Dengue. Just before Christmas, it made an Investigational New Drug (IND) application to the FDA, seeking permission to start the clinical trial. The company told shareholders it would expect an answer in 30 days.

This answer has come, but it was not the one shareholders wanted.

 

It wasn’t good news

The FDA did not approve the IND, instead placing it on Clinical Hold and telling the company that it would need to alter the protocol and the IND in order to advance the program.

Island told shareholders it was working with vendors and consultants to formulate the best plan. Shareholders are evidently not optimistic, as the 25% share price decline in the last fortnight suggests.

 

 

Mesoblast is working on a resubmission too

Mesoblast is at a later stage to Island Pharmaceuticals, having already conducted clinical trials for its Remestemcel-L stem cell treatment. 

The company is now trying to obtain FDA approval for remestemcel-L for steroid-refractory acute graft versus host disease. The company was first knocked back in September 2020 and it has been trying to obtain approval ever since.

Mesoblast has told shareholders that it made its case to the FDA once again and that it had addressed the FDA’s concerns. Investors will need to wait up to six months for the results, because this is the maximum period the FDA takes to review a submission. Oh well…more waiting.

 

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