Eiger BioPharmaceuticals: Peginterferon Lambda COVID-19 Data Very Positive

Leonard Yaffe profile picture
Leonard Yaffe
2.67K Followers

Summary

  • On October 15, Eiger announced results of a Toronto General Hospital investigator-sponsored study in outpatients with mild to moderate COVID-19.
  • As was seen with the Regeneron data for its monoclonal antibody cocktail, patients with a high baseline viral load demonstrated a statistically significant benefit in time to viral clearance.
  • Given that lambda is well tolerated and easy to administer, I would expect the drug to become widely used as first line therapy if further studies support these results.
  • In a July article, I suggested that Eiger could achieve EPS exceeding $25 per share with successful commercialization of lambda for COVID-19.

Eiger BioPharmaceuticals (EIGR) announced today results of the Toronto General Hospital ILIAD study in outpatients with mild to moderate COVID-19. Sixty patients were randomized 1:1 to a single subcutaneous dose of Lambda 180 mcg or saline. For those patients with a baseline viral load greater than 6 log copies per milliliter, 15 of 19 patients in the Lambda group were virus negative at Day 7 versus 6 of 16 in the placebo group. This translated to a median time to viral clearance of seven days for Lambda and ten days for placebo.

In the US, there are currently 45,000-50,000 daily new COVID-19 cases diagnosed, up from 30,000 six weeks ago. This can largely be attributed to the opening of schools and restriction relaxation in several states. I had previously forecast daily new infections to decline to 20,000 by late fall, but this now seems optimistic. At 30,000 cases per day, this equates to 900,000 cases per month, or over 3.5 million cases by March. I note that Gilead is charging $3,000 for a five day course of remdesivir, which demonstrated faster recovery times and is focused on moderate to severe COVID-19 patients. More infected people would fall into the ambulatory market, and it is critical to realize that the viral load would not be ascertained for several days after diagnosis. Therefore, the possibility exists for Lambda to be prescribed to this patient group independent of viral load, given its safety profile and subcutaneous administration, although the pricing would have to be appropriate.

I have recently been fortunate to speak with several leading COVID-19 experts, and the predominating opinion is that a vaccine will become widely available in the US in the March-April time frame. The main concern relates to the duration of conferred immunity. In the meantime, they expect new daily cases of around

This article was written by

Leonard Yaffe profile picture
2.67K Followers
I am an MD by background who runs a healthcare hedge fund. I worked as a sell-side medical analyst for 20 years, covering pharmaceuticals, medical devices, PBMs and drug distributors.

Analyst’s Disclosure: I am/we are long EIGR. I wrote this article myself, and it expresses my own opinions. I am not receiving compensation for it (other than from Seeking Alpha). I have no business relationship with any company whose stock is mentioned in this article.

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