Merck
Serono pulls development of lung cancer prospect
The company, which is the
biopharmaceutical division of Merck KGaA, announced today that it has ended a
study programme investigating tecemotide as a monotherapy in stage III
non-small cell lung cancer (NSCLC) after poor results from a trial involving
Japanese patients.
The phase I/II trial,
known as EMR 63325-009, compared tecemotide to placebo in patients on
concurrent or sequential chemoradiotherapy. Results from the study suggested
tecemotide had no effect on the primary endpoint of overall survival or any of
the secondary endpoints.
Luciano Rossetti, global
head of research & development at Merck Serono, said: “While the data from
the exploratory subgroup analysis in the START trial1 generated a reasonable
hypothesis to warrant additional study, the results of the recent trial in
Japanese patients decreased the probability of current studies to reach their
goals.”
Instead Merck Serono will
turn its attentions to other cancer prospects, with Rossetti singling out
fellow immunotherapy MSB0010718C as a priority for the company in lung cancer.
MSB0010718C is one of
several promising anti-PD1 immunotherapies currently in development by pharma
companies for a variety of cancers.
The most advanced
treatments in this class are Merck & Co's pembrolizumab, which was recently
approved in the US under the brand name Keytruda to treat melanoma, and
Bristol-Myers Squibb and Ono's nivolumab, which has a similar approval in Japan
under the brand name Opdivo.
With the melanoma market
already looking very competitive, Merck Serono has prioritised the development
of its anti-PD1 in other cancers, including metastatic Merkel cell carcinoma
(MCC) for which the drug is in phase II trials.
Lung cancer is another
promising area for the drug and Merck Serono plans to investigate the drug in a
number of other cancers, including colorectal cancer, breast cancer and
prostate cancer.
As for the future of
tecemotide, Merck Serono has not ruled out the drug's potential in other forms
of cancer, and the company will continue to supply the immunotherapy for
ongoing investigator-sponsored trials in other indications.
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