BPAX addendum: It’s a shame that such impressive clinical data had to be marred by a classic Rodman & Renshaw swindle. The timing of the BPAX’s two PR’s—8am ET for the clinical data and 2:16pm ET for the financing—allowed investors who bought into the financing to short BPAX with abandon all morning and half the afternoon.
I didn't catch the link to Antares (symbol: AIS) when you first posted this and only caught the connection upon digging into BPAX a little more. Do you know anything about Antares? They are a similarly sized drug company (~$65 million market cap). Here's a link to their Web site: http://www.antarespharma.com/index.html . They've been around for awhile and were formerly known as Medi-Ject Corporation.
Anyways, apparently BPAX licensed the U.S. rights to LibiGel from AIS while AIS maintains all rights ex-U.S. Per the 2Q09 AIS conference call I just listened to, AIS is entitled to 25% of any sub-licensing fees BPAX receives from licensing the U.S. rights to LibiGel, plus royalties. I would be curious to know what U.S. royalty rate AIS is entitled to as the 25% figure appeared to be strictly related to sub-licensing fees and not also royalties.
Antares has a lot more going on than LibiGel as the FDA just approved the Tev-Tropin Tjet Injector system (human growth hormone delivered in a needle-free injection system). AIS sells the device to Teva and is also due royalties on the sales of Tev-Tropin Tjet. They also have a Phase 3 compound for overactive bladder called Anturol (oxybutynin delivered via AIS' proprietary ATD gel) that they expect to partner in the next 6-9 months. Finally, they indicated they have enough cash to last 12 months based on current cash balance and expect to launch one product per year for the next 5 years.
BPAX/LibiGel more safety data in Phase III program
An independent data monitoring committee reviewed all unblinded adverse events in the safety study of LibiGel. There have been no deaths, one myocardial infarction and three breast cancers reported in the study. The committee recommended the continuation of the trial.