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Friday, August, 29, 2008

Me-too and me-three drugs

by  Dr. Bill Quick
Saturday, February 02, 2008
Dr. Bill Quick
Dr. Bill Quick
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Dr. Bill Quick and his wife Steph are the authors of one of the ...

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Last month, there was a flurry of news stories that a new diabetes drug was being developed. Sounded wonderful, but it turned out to be just another me-too/me-three drug situation.

Turns out that a Japanese drugmaker, Takeda, has been developing a drug called alogliptin, and has recently applied to the FDA for approval to market it in the US for type 2 diabetes. Looking at the story, it turns out that alogliptin is another in a long line of "DPP-4 inhibitors" that are either on the market (Januvia, made by Merck) or in development (including Galvus from Novartis, saxagliptin AKA BMS-477118 from BMS, Redona/denagliptin from GSK, and others).

Januvia (sitagliptin) was the first DPP-4 inhibitor to become available on the US market. It was approved for the treatment of type 2 diabetes in the United States in October 2006, and has been a commercial success, as its once-daily dosing and lack of major side effects (such as lack of hypoglycemia and lack of weight gain) have been selling points -- even though it's been considered minimally efficacious (that is, the drop in A1C is not impressive), and it's expensive compared to older drugs such as metformin.

Approval of Novartis's DPP-4 inhibitor, Galvus (vildagliptin), had actually been expected before Januvia, but Galvus was delayed after the FDA requested more data showing that skin lesions that had been seen in monkey tests don't occur in people. Further studies are furiously underway by Novartis to try to answer the FDA's concern. In Europe, by the way, Galvus has been approved for sale.

Along with the other DPP-4 inhibitors being developed, it should be noted that Takeda has another DPP-4 inhibitor, which is called SYR-472. SYR-472 is being positioned as back-up and possibly a next-generation drug, according to news stories.

So, what's going on here? Clearly there's a market for what are sarcastically called me-too (second to market) drugs, and me-three (third to market) drugs. So there's a race to get these drugs through the laborious and expensive clinical trials that are required to get approval, and to share the market with the first drug out of the gate. And if the leader stumbles, as Galvus did with the monkey problem, then the putative second-place finisher might jump into the lead, as Januvia did in this class of drugs.

But is there a market for the fourth, or fifth, or sixth drug? Turns out that there is, even though many me-too and me-three drugs are really no better and no safer than the first one. Apidra (insulin glulisine, from sanofi-aventis), for instance, hasn't caught the eye of physicians, as Humalog (insulin lispro, from Lilly) and Novolog (insulin aspart, from Novo-Nordisk) had a huge head start getting to market, and to date, I'm unaware of any data showing Apidra is any better or safer than the other two rapid-acting insulin analogs. And sadly, it's not being promoted as being cheaper -- the second and third drugs rarely try to compete on price, even when there's generic competition. There even could be a me-four insulin in the USA: Wockhardt, a company based in India, has a similar product that they sell in other countries, and on their website, they say that the US "is one of the key focus areas for the company's growth strategies."

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