Shares of Ligand Pharmaceuticals LGND are down again following the results of the Phase III trial of Promacta.
GSK Releases Promacta Phase III Results
In a press release from June 13, GlaxoSmithKline announced the results from the “Phase III PETIT2 study evaluating the efficacy of eltrombopag vs. placebo in paediatric patients with chronic immune (idiopathic) thrombocytopenic purpura (cITP).”
Eltrombopag, known as Promacta in the U.S. and Revolade in Europe and other countries, met the primary endpoint in the study. The results showed a “statistically significant improvement in platelet counts with almost 40 percent of patients treated with eltrombopag attaining a consistent platelet response for 6 of 8 weeks compared to placebo (39.7 percent vs. 3.4 percent, respectively, p<0.001).”
“The PETIT2 study results presented today show an increase in platelet response rate with eltrombopag treatment— an important result given that these children had failed other standard therapies,” said Dr. Rafael Amado, Head of Oncology R&D, GlaxoSmithKline. “We look forward to continuing to assess the potential of eltrombopag in these patients and to moving forward with planned regulatory submissions for a paediatric indication in cITP later this year.”
Seeking Alpha Sees “Extreme Downside” for Ligand
The financial media outlet noted 100 percent downside for shares of Ligand. Seeking Alpha highlighted three main points in its article on Monday:
Market News and Data brought to you by Benzinga APIs- Revenue and profits highly concentrated in one (single-sourced) product, and essentially two royalty agreements, one of which is set to decline precipitously.
- Based on recent FDA comments, Gilead's revolutionary Sovaldi drug will virtually eliminate demand for Promacta, which is Ligand's largest royalty generating asset, accounting for as much as 72 percent of Ligand royalty revenue as recently as Q4 2013.
- When backing out intangibles from the balance sheet, net shareholder equity is approximately minus $4 million.
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