Why Investors and Traders Need to Track Content Of Prescription Drug User Fee Act

 | Jun 02, 2021 12:53PM ET

Dates and content of the Prescription Drug User Fee Act are essential for portfolio managers of health-care stocks. A single positive or negative announcement from the U.S. Food and Drug Administration (FDA) can send shares of a biotech firm soaring or turn a hot name quickly into a bear market. Among the dozens of corporate event data points provided to our customers, Wall Street Horizon gathers PDUFA dates and content so our clients stay in the know.

PDUFA Details And Market Impact

Specifically, a PDUFA date is the goal date set by the FDA for announcing its decision on a company’s New Drug Application/Biologics License Application/ Supplemental Biologics License Application (sBLA)/ Supplemental New Drug Application (sNDA) after reviewing applications. Traders should be aware that the FDA may rule before the announced PDUFA date. PDUFA dates can even fall on weekends.

Pharmaceutical companies, particularly small biotech companies, can experience significant volatility around PDUFA dates. One of the stocks we feature in this report rallied following positive news, but then recently experienced a gap-down in price associated with a delay in the FDA review process for a key drug in its pipeline.

Viewing PDUFA dates and content along with additional corporate event data allows money managers to see the crucial events on the “horizon.”

Why It’s Different This Time

2020 was a year we will never forget for reasons beyond trading. The last 15 months might have marked a turning point in the health-care sector specifically regarding the drug development and approval process. The FDA even said that 2020 was a strong year for drug therapy approvals despite the focus on COVID-19. The vaccines were fast-tracked by the FDA, and the process was generally smooth despite small hiccups such as the Johnson & Johnson vaccine pause earlier this year.

Industry experts are optimistic that an outcome of the COVID-19 pandemic will be enhanced cooperation among drug companies, researchers, hospitals and regulators. The lessons learned from the process of researching, developing, performing clinical trials, approving and administering the shots might also remove silos that once existed, according to some.

The post-COVID world could feature increased pharmaceutical company drug development and the potential for more efficient and effective FDA oversight. The result could be more drug manufacturers requesting approval from the FDA, hence more PDUFA dates for traders to monitor.

The trend of speeding up drug approval is nothing new. It is how PDUFA dates came to existence in 1992. The process used to take about 30 months before the 1992 PDUFA law, which we detailed in our 2018 piece .

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FDA Drug Approval Process Dates To Track

It is important to understand that the following dates represent stages of drug trials, and it may mean there are content updates available as well. Investors can view source documents to read firsthand about the PDUFA update.

PD Start – Date the drug manufacturer submits its NDA

PD Expect – Date the FDA is expected to respond to the drug manufacturer with its approval/non-approval

PD Update – Dates for any/all events that occur during the review process, e.g. FDA updates, changes to the Expect date, etc.

PD End – Date the FDA responds to the drug manufacturer

Companies In-Play With Upcoming PDUFA Dates

Within the small and mid-cap biotech space, Omeros Corporation (NASDAQ:OMER) recently had its Transplant-Associated Thrombotic Microangiopathy (TA-TMA) drug Narsoplimab pushed back three months from mid-July to mid-October.

Omeros is a biotech firm with a market cap slightly under $1 billion. The Seattle-based company and Nasdaq-listed stock has been a strong performer since Q3 2021 as traders grow more optimistic regarding upcoming drugs. Management believes Narsoplimab plays a role in growing its diversified pipeline.

On Jan. 19, 2021, Wall Street Horizon reported OMER’s PDUFA target action date of July 18. On May 20, however, OMER announced that the FDA will require additional time to review the BLA for Narsoplimab. The new PDUFA target action date is Oct. 17, 2021. As this date falls on a weekend, we expect the PDUFA decision on the preceding Friday. Wall Street Horizon provided clients a link to the Omeros press release so they can investigate the news further.