Burrill captures a broad swath of healthcare M&A activity in its database. Looking more narrowly, "bio-pharma" M&A has been almost non-existent this year: AstraZeneca (AZN) bought Omthera Pharmaceuticals; Allergan (AGN) bought MAP Pharma; we've seen some private companies gobbled up, but that's it.
Transformational, head-turning deals --
(GILD) buying Pharmasset for $11 billion, for example -- have not materialized this year.
It's impossible to pinpoint precisely the reason(s) for the drop off in biopharma M&A this year, but the biotech bull market is a likely culprit. Think about it, biotech and drug -- companies, regardless of quality, are expensive right now, making it more difficult for potential acquirers to make deals work financially. Factor in takeout premiums and there's probably a lot of potential buyers out there suffering from sticker shock.
I view initial public offerings as the flip side of the M&A market and they're booming like never before. Seventeen healthcare IPOs have already hit the market this year with another 18 companies in registration, according to Burrill.
@adamfeuerstein $QCOR What's your opinion on Synacthen rights acquisition fr. Novartis?— hakahaka (@hakahaka) June 11, 2013I have rarely weighed in on the bull-bear debate that rages over Questcor Pharmaceuticals (QCOR). Generally, I view Questcor's business model -- with respect to Acthar pricing and marketing -- to be slimy but smart and legal. Questcor identified loopholes and gray areas within the law and took advantage of them to make a lot of money off an old drug. Questcor is not the first drug company to operate in this manner and it won't be the last. In the past year, Questcor's Acthar marketing practices have come under a lot of scrutiny from insurance companies, some of which are pushing back. At the same time, Acthar sales continue to grow, which has helped Questcor's stock price regain almost all the losses suffered last fall. Along the same lines, I view the Synacthen acquisition as another smart and duplicitous move by Questcor management. By buying Synacthen from Novartis (NVS), Questcor pockets a potential competitive threat to Acthar. The purchase agreement includes language to compel Questcor to develop Synacthen and seek U.S. approval. You're totally naive if you believe Questcor will ever do such a thing. The company will find a way to bury Synacthen in a deep hole, even if it requires paying financial penalties to Novartis. One year ago, this is how Questcor Chief Scientific Officer David Young spoke about Synacthen: With respect to Synacthen, a synthetic peptide marketed by Novartis in Europe and Australia. We believe unlikely to be competitive to Acthar. Synacthen is a fragment of ACTH called tetracosactide and is not an androgynous peptide of the body. It has the different amino acid sequence and a different pharmacology profile from Acthar Gel. Synacthen contains benzyl alcohol, which is toxic to children, it can potentially cause gastric syndrome, it can be fatal. Since Acthar Gel is widely used in children under 2 years of age for infantile spasm, Synacthen might face substantial safety and distribution issues in U.S. In addition, Synacthen would face the same regulatory and business issues discussed earlier for similar ACTH trials... This week, Questcor CEO Don Bailey sings Synacthen's praises: As an emerging leader in melanocortin research, we now have the opportunity with Synacthen to expand and accelerate our product development activities. We believe such efforts will enhance our expanding R&D program. In addition, this key acquisition provides an opportunity to initiate our presence in more than three dozen international markets, giving us an opportunity to reinvigorate Synacthen in these markets and providing us a platform for potential international growth. Adds Young: We intend to develop and seek FDA approval for Synacthen and are committed to developing this product not only in conditions different than Acthar but also in conditions where Synacthen would potentially provide a clinical benefit over Acthar. Proof that investors should think twice before believing anything that emerges from the mouths of drug company executives.
Pierre G. writes: Last month you had a piece about Celsion (CLSN) and I completely disagree with you. Yes, to the extent that Celsion management made a mistake using such a large study group but it would seem that when involving just the subgroup mentioned, data are substantially different. Have you changed your opinion here? Pierre is referring to my column -- Celsion's Shameless Spin Job -- published in April. Thermodox failed. End of story. Don't buy Celsion on the hope this liver tumor therapy can be resurrected. It won't happen. Celsion is trying to convince you otherwise, assisted by a small cadre of clueless stock promoters on Seeking Alpha, but don't listen to them. Thermodox doesn't work. The data don't lie: These curves plot progression-free survival (PFS) for the two treatment arms of Celsion's pivotal "HEAT" study: Thermodox plus radio-frequency ablation (RFA) versus RFA alone. PFS was the study's primary endpoint. Trust me, there are two curves on that graph. It's hard to tell because they sit right on top of each other, meaning Thermodox is a placebo. The therapy had no benefit at all for patients with liver tumors. The survival curves from the HEAT study look exactly the same as the PFS -- completely overlapping, no benefit whatsoever demonstrated for Thermodox. "HEAT" was a large and well-conducted study. The conclusions are definitive. Thermodox doesn't work. Yet Celsion persists in misleading investors with post-hoc looks at arbitrary subgroups of patients. The company claims Thermodox may benefit patients who underwent more than 45 minutes of RFA therapy. Why 45 minutes? Why not 30 minutes or an hour? There is no scientific rationale for why 45 minutes or more of RFA therapy would make a difference and Celsion doesn't offer any. Celsion chose the 45-minute cut off because that's where the fake re-analysis looks best for stock promotion purposes. This slide, a version of which I published in April, debunks the 45-minute RFA story: You're looking at the pharmacokinetics of Thermodox. In other words, how much Thermodox gets into a patient's bloodstream following RFA treatment. What you see, clearly, from the graph is patients get the vast majority of Thermodox in the first 45 minutes of RFA treatment. Extending RFA treatment beyond 45 minutes isn't going to expose tumor cells to more Thermodox, which means Celsion's post-hoc analysis is bunk. Seeking Alpha contributor "Alpha Exposure" published a smart takedown of Celsion this week that's worth reading. Celsion's response to the article was lame. I'd also read Alpha Exposure's rebuttal posted Thursday. -- Reported by Adam Feuerstein in Boston. Follow Adam Feuerstein on Twitter.
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