Health and Healthcare

4 Major FDA Decisions Expected by June

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Pharmaceutical companies generally are involved in the lengthy process of getting their drug candidates to market through clinical trials. There is a fair amount of risk to a great amount of risk involved, as with biotech companies, should a study come back negative or should a candidate not be approved. Conversely, if a drug is approved or passes a clinical trial, there can be massive upside.

The long and short of the matter is that U.S. Food and Drug Administration (FDA) rulings can make or break these companies.

24/7 Wall St. has collected several big FDA decisions that should be coming up in the June quarter and added some color, along with the trading range and price target.

Note that, due to many outside and internal factors, there are no assurances that the dates will remain static. Some date changes are positive developments, and some can be disasters if a company is not deeply financed.

As a side note about the Prescription Drug User Fee Act (PDUFA): a Priority Review designation is granted to medicines that the FDA determines have the potential to provide significant improvements in the treatment, prevention or diagnosis of a disease.


Sarepta Therapeutics Inc. (NASDAQ: SRPT), despite facing setbacks earlier this month with an FDA panel, is still going forward with its PDUFA date later this month (May 26). This has the potential to make or break Sarepta. The problem that it faced earlier was that Sarepta did not live up to FDA guidelines in this trial, and the company was ultimately questioned over it.

The FDA panel voted against recommending it for approval, although the patients within the trial pleaded for its recommendation. With that said, this PDUFA date will signal if these pleas were heard, and should the decision go one way or the other, we can expect a massive move within the stock.

Jefferies recently issued a mere $7 price target. Its research call in the first week of May said:

We see likely a new eteplirsen Phase 3 study would be required for approval and low probability of accelerated approval & 55% probability of positive Phase 3 data and launch by year-end of 2020 for eteplirsen in DMD… Eteplirsen should take meaningful market share given good safety profile if approved.

Shares of Sarepta closed Friday at $17.70, with a consensus analyst price target of $17.92 and a 52-week trading range of $8.00 to $41.97.

AstraZeneca PLC (NYSE: AZN) has a potential best-in-class treatment for hyperkalaemia, a condition associated with increased mortality in patients with chronic kidney disease, diabetes mellitus and chronic heart failure.

Currently the treatment, ZS-9, or saxagliptin/dapagliflozin, is under regulatory review by the FDA with a PDUFA goal date in late May. AstraZeneca also has a submission for European Marketing Application Authorisation that is also progressing as planned.

AstraZeneca shares closed Friday at $27.96, with a consensus price target of $35.41 and a 52-week range of $27.68 to $35.34.

Ariad Pharmaceuticals Inc. (NASDAQ: ARIA) is gearing up for the American Society of Clinical Oncology (ASCO) annual meeting, where the company will present data on its Phase 2 ALTA trial of brigatinib. The annual meeting is set to start on June 3.

In addition to an anticipated data presentation at ASCO, Ariad believes that it is on track to file for approval of brigatinib in the United States in the third quarter of this year. Brigatinib has received breakthrough-therapy designation from the FDA.

Be advised that Ariad had once been considered a potential buyout target, but that has been about a year ago. Its shares were also closer to $10.00 back at that time.

Shares of Ariad closed Friday at $6.98, with a consensus price target of $8.25 and a 52-week range of $4.37 to $10.07.

BioMarin Pharmaceutical Inc. (NASDAQ: BMRN) announced this past week that the European Medicines Agency (EMA) granted the request for accelerated assessment for the Marketing Authorization Application for cerliponase alfa. However, the company expects to submit cerliponase alfa for a Biologics License Application to the FDA by mid-year.

Analysts recently weighed in on BioMarin after its earnings:

  • BMO Capital Markets raised its price target to $108 from $107.
  • Cowen has an Outperform rating with a $150 price target.
  • JPMorgan has an Overweight rating and raised its price target to $120 from $117.
  • Oppenheimer maintained a Perform rating with a $99 price target.

Shares of BioMarin closed Friday at $80.80, with a consensus analyst target of $114.79 and a 52-week range of $62.12 to $151.75.

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