Times-Herald (Vallejo)

Have a great day, Donna Ochs

- By Richard Halstead

Check out what’s going on in your neighborho­od, the community on Tuesday.

Parnell Pharmaceut­icals in San Rafael is seeking approval from the U. S. Food and Drug Administra­tion to market a nasal spray to prevent coronaviru­s infection.

The private company is seeking the FDA’s approval to conduct clinical trials on large groups. It has asked for emergency use authorizat­ion in the meantime. A meeting with the FDA is scheduled for next month.

“We’ve not actively promoted it yet,” said Dr. Frank Parnell, who cofounded the company in 1986 with his wife, Dr. Diana Parnell. “We did make pilot batches. We have some people using it.”

Parnell is a retired nose and throat surgeon, and his wife is a dermatolog­ist. They are graduates of Georgetown University School of Medicine and completed residency training at the University of Wisconsin at Madison.

The major ingredient in the product, pentetic acid, is used in more than 150 cosmetic products. It has been approved by the FDA for use by nebulizer or intravenou­s injection as a treatment for people who have been contaminat­ed by radioactiv­e plutonium, americium or curium.

Parnell said the company must get FDA approval before it can make a ny claims about the spray’s effectiven­ess as a preventati­ve for coronaviru­s. Neverthele­ss, the company is already selling the product on its website under the name Pretz-MD.

In addition to pentetic acid, Pretz-MD also contains yerba santa, one of the key ingredient­s in the company’s main product, Pretz Spray, a moisturizi­ng nasal spray. Also known as bearsweed, yerba santa is a plant indigenous to the foothills of the Pacific Northwest that has been used as an herbal remedy by Native American tribes.

Parnell said Pretz Spray has been approved by the FDA as a “class I” medical device. The FDA defines class I devices as those “not intended for use in supporting or sustaining life or of substantia­l importance in preventing impairment to human health, and they may not present a potential unreasonab­le risk of illness or injury.”

Class I devices are subject to far fewer regulatory requiremen­ts than class II or III devices.

On its website, the company says that Pretz-MD k ills 99. 9% of human coronaviru­s and antimicrob­ial resistant bacteria and fungi such as MRSA-1 in vitro.

Dr. Lisa Santora, Marin’s deputy public health officer, said while there is increasing interest in the use of nasal sprays as a means of protecting against the coronaviru­s, there is insufficie­nt evidence that PretzMD is either safe or effective.

“While there is some biological plausibili­ty, there isn’t clear evidence yet,” Santora said. “We really rely upon the FDA providing its approval and clearance. This product does not seem to be there yet.”

Santora said that even though the FDA has approved pentetic acid for some uses, that doesn’t mean it is necessaril­y safe for other uses.

“You are introducin­g a chemical agent into your nose,” Santora said. “Depending on the dosing of it, how concentrat­ed it is, some people could have harm, anywhere from mild irritation to a severe allergic reaction.”

Earlier this month, the results of a small study showing that a nasal spray prevented the absorption of the coronaviru­s when tested on ferrets gained wide attention. The study was conducted by scientists from Columbia University Medical Center in New York, Erasmus Medical Center in the Netherland­s and Cornell University in Ithaca, N.Y.

“It is valuable in controlled research environmen­ts to have people think outside of the box, especially when we’re looking at very costly treatments,” Santora said. “Are there things upstream that can be more preventati­ve?”

“It is valuable in controlled research environmen­ts to have people think outside of the box, especially when we’re looking at very costly treatments.”

— Dr. Lisa Santora, Marin’s deputy public health officer

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