Exhibit A? I am flat out jazzed, for Whitehouse Station! More precisely, I am just frothy with anticipation -- about the future prospects of MK-3475, or lambrolizumab, if you prefer. It is a stunningly new way of fighting cancer. It does so essentially by removing the natural "brake" built in to our own immune systems (see graphic at right; it was derived from this fine article). MK-3475, it is thought, blocks a specific T-Cell "down regulator" -- and that allows our bodies' immune system to fire machine-gun fashion, at specific tumor cells. Rather than cock and reload and aim and fire -- this (it is thought) converts the bodies' own anti-cancer weapons into a "Gatling gun", on the fly. That is, it amps up our own counter-attacks -- and leaves healthy cells unpreturbed (or so the early data might suggest). [Now, to be fair, Bristol Myers Squibb has a prior in time anti-PD-1 candidate in its pipe, one called nivolumab, and it may actually beat Merck to market -- clear FDA review -- as to at least some oncology indications.] Even so, there will be "plenty of pie," to go around -- if this approach works as well as it would seem it might. The oncology markets currently targeted by the two companies, independently, rake in perhaps $45 billion per year, in the aggregate -- with what appear to be significantly less effective on-market drugs. [Backgrounder here.]
Of course, as with any biotech approach, a million things could still go wrong -- for example, the longer term effect might be that the patient's immune system goes haywire, generally, over time -- and starts attacking healthy cells, indiscriminately. That's not likely (given graphic at right), but it is at leat remotely possible. The reply would be that in end-stage cancer patients (where the bio-tech will be initially deployed), these patients are likely to die within six months, in any event. And if the treatment works, they may gain a minimum of two to five more good years.
That sort of survival benefit will compel the world's various versions of reimbursement machinery to pay a perhaps quite hefty premium for nivolumab and/or lambrolizumab. But let's not get too far ahead of the story. The story right now is a horse race -- and in a nice piece by the U.K. based PharmaTimes, we are treated to some of the detail, about Merck's three additional entries:
. . . .With Pfizer, Merck will assess in Phase I/II clinical studies the safety and efficacy of MK-3475 in combination with the former's small molecule kinase inhibitor Inlyta (axitinib) in patients with renal cell carcinoma, and separately MK-3475 plus PF-05082566 (PF-2566), an investigational immuno-oncology agent that targets the human 4-1BB receptor, in multiple cancer types.
Incyte and Merck will collaborate on a randomised, double-blind placebo controlled Phase I/II study to evaluate the safety andefficacy of a regimen combining MK-3475 with Incyte’s investigational immunotherapy agent INCB24360 in patients with previously-treated metastatic and recurrent NSCLC, among other advanced or metastatic cancers.
Amgen and Merck will look at MK-3475 in combination with Amgen’s investigational oncolytic immunotherapy talimogene laherparepvec in a Phase I/II study in patients with previously untreated advanced melanoma.
MK-3475 is an investigational, highly selective anti-PD-1 immunotherapy which is designed to restore the natural ability of the immune system to recognise and target cancer cells, and analysts are expecting the drug to make peak sales of at least $2 billion if it makes it to market. . . .
To be sure, this spend in the near term, at Merck, is not small. The three above, plus the two previously-announced, likely place the quarterly spend on the MK-3475 clinical trials at $1 billion. Or about $4 billion on the year 2014. If Merck hits solid doubles in four or five of these, though -- that $2 billion a year in projected revenue might be closer to $6 or $8 billion, a year. Overall most analysts still figure BMS's nivolumab will reach between $6 and $12 billion. A year. And (if approved at FDA) it is not likely that the pie will shrink much, when Merck enters. There is just that much pent up demand for a truly effective, time-of-survival enhancing approach -- for cancer patients in the renal, melanoma and lung (and later -- in the bone and blood) cancer arenas. Now we wait for the end of May/first of June, 2014, and ASCO in Chicago -- when the next big data sets, on anti-PD-1, will be out.








