NEBIDO

An Overnight 2-Bagger
By Brian Orelli
September 29, 2008 Comment (0) Recommend (0)
You've got to love drug development. Where else can you see stocks double overnight?

Indevus Pharmaceuticals (Nasdaq: IDEV) looked like it was down and out after the Food and Drug Administration said it wanted more safety data about a rare side effect of its long-acting testosterone substitute, Nebido. But it looks like the agency won't require additional clinical trials after all. Instead, Indevus will be allowed to submit data from trials in the U.S. and Europe to explain why the drug should be approved despite short-term coughing episodes that occur immediately after some injections when a small amount of the oily solution containing the drug enters the bloodstream. The share price doubled on Friday in response.

The drugmaker will submit the data during the first quarter of next year and hopes it will have Nebido on the market by the end of the year. Ahh, what a difference a few months make!

Adding fuel to the fire, Indevus announced that it partnered with Teva Pharmaceuticals (Nasdaq: TEVA) to develop its phase 2 compound pagoclone, which treats stuttering. The partnership allows for either a 50/50 split, with Teva paying Indevus up to $92.5 million in milestone and research reimbursement payments, or it can be transformed into a royalty stream. While complicated, the structure of the deal could give Indevus some flexibility should it start running low on funds.

I like Teva's move to expand the number of name-brand drugs it sells. The generics-plus strategy, which Mylan (NYSE: MYL) recently decided to stick with, allows generic-drug makers, like Barr Pharmaceuticals (NYSE: BRL) and Par Pharmaceutical (NYSE: PRX), to sell higher-margin branded drugs to supplement their lower-margin generic business. It's clear that the two can coexist -- even pharmaceutical companies like Novartis (NYSE: NVS) and Sanofi-Aventis (NYSE: SNY) are making it work.

Turning back to Indevus, while the pair of announcements last week are certainly good news and the company deserves the higher market cap (as I said it did in June), Indevus isn't out of the woods yet. The FDA has agreed to accept the data, but that's still a long way from an approval. And pagoclone has another phase 2 and a couple of phase 3 trials to go before we'll know if it'll be a success.

Indevus could easily double again from here, but with that potential for reward comes lots of risk. Tread lightly, Fools.
 








Here is the reply from ENDO IR department on aveed and octreotide

Good Morning xxxxxx,

We provide regular updates on the status of those programs through our SEC filings and scheduled events such as quarterly earnings calls.

Our most recent updates on AVEED would be that during the second quarter we met with the FDA regarding the path forward for Aveed, our long-acting injectable testosterone. We are currently considering the outcome of that meeting and our next steps. However, we will have to complete that evaluation before commenting further. The good news is a US patent covering the formulation of Aveed issued on May 18, 2010 (patent number 7,718,640) and will expire March 14, 2027.

Our most recent updates on Octreotide would be that the phase III study for the treatment of Acromegaly completed full enrollment during second quarter. We expect to begin review data from this trial by late this year or early-2011 and if warranted by the results we could be in a position to submit an NDA by mid-2011.

Thank you,
Jonathan Neely
Associate Director
Investor Relations
 








Endo shares sink after FDA rejects Aveed NDA


December 3, 2009 | By John Carroll


Shares of Endo Pharmaceuticals (ENDP) slid this morning after investors got wind of the news that the FDA stiff-armed the company's application to market its new drug for low testosterone. Low testosterone is associated with a variety of ailments, including fatigue and loss of libido.

Regulators want more information on rare but serious incidents of anaphylactic reactions and pulmonary oil microembolism among patients taking Aveed (known as Nebido outside the U.S.). And the FDA said in its complete response letter that Endo's risk mitigation program for the drug is inadequate. Endo stock was down nine percent in premarket trading.

The FDA's rejection marks a setback for Endo CEO David Holveck, who recently signaled his interest in a new round of deals to help the company expand beyond pain into new therapeutic areas like cancer. Earlier this year Endo bought out Indevus for $370 million, winning Aveed in the deal. Holveck is now looking for new licensing pacts, acquisitions and development deals. In a terse release, the developer says that it's evaluating the FDA's letter.