Johnson & Johnson loves to make ambitious pronouncements for itself. Its latest was a commitment to submit to the FDA applications for 10 potential blockbusters within five years by the end of 2019. It fleshed out where it is on those 2015 plans on an Oct. 18 conference call.
In the longer term, the pharma is also making some overtures in immuno-oncology, an area that hasn’t explicitly been a major part of its strategy. J&J has been investing in “four critical areas including vaccines, T cell checkpoint inhibitors, T cell redirection and myeloid mechanisms of action,” said the company’s global head of pharmaceutical R&D, Dr. William Hait, during the call.
He said the pharma has 15 immuno-oncology assets in development, including eight that are already in the clinic.
“While we did not explicitly address immuno-oncology during our 2015 Pharmaceutical Business Review, we continue to make significant progress in this area,” said Hait. “We currently have 15 immuno-oncology assets in development, including eight that are in the clinic. Recently, we uncovered an important additional mechanism of action of Darzalex to the immune-mediated through the depletion of immunosuppressive myeloid and lymphoid populations including a previously unrecognized supersuppressor CD38 positive T-reg population as well as activation of CD8 and CD4 positive effector T cells. These results provide the impetus for exploring Darzalex in indications beyond key malignancies in solid tumors.”
Darzalex is the first of the 10 new potential blockbuster molecular entities J&J committed to filing; the CD38 monoclonal antibody to treat double refractory multiple myeloma was approved by the FDA last year. Up next is sirukumab to treat rheumatoid arthritis, for which it has already filed, and guselkumab for psoriasis for which it plans to file before year end.
On the immuno-oncology front, J&J partnered earlier this year to take its early stage antigen-presentation treatment into Phase II testing in combination with Opdivo (nivolumab) from Bristol-Myers Squibb.
Last year, Swedish startup Alligator Biosciences also did an immuno-oncology deal with J&J worth up to $700 million in milestones and royalties. It has a CD40-targeting ADC-1013, an antibody designed to spur a T-cell attack on cancer.
J&J also partnered with another startup in that time frame–San Diego,CA-based Poseida Therapeutics–to discover and develop new CARs, T cells and natural killer cells adapted with chimeric antigen receptors and targeted at cancer cells.
Slow growth in hepatitis C and the promise from Pfizer that a biosimilar Remicade is coming to market later this year were both downplayed by J&J. Remicade is by far J&J’s biggest drug with $5.3 billion in sales during the first three quarters of this year.
By Stacy Lawrence
Source: Fierce Biotech
Hybrid closed-loop systems rely on an algorithm to first analyze real-time blood sugar readings from a continuous glucose monitor, then use the results to adjust an insulin pump’s output as needed throughout the day. In this case, the algorithm was developed by Diabeloop, the CGM is a Dexcom G6 sensor, and the insulin pump comes from ViCentra.
Boehringer Ingelheim has acquired bacterial cancer therapy company T3 Pharmaceuticals in a deal that could be worth up to 450 million Swiss francs ($508 million). The addition of Allschwil, Switzerland-based T3 will “significantly expand” the German drugmaker’s immuno-oncology pipeline and aligns with some of the company’s existing R&D programs.
EuroAPI has completed the acquisition of BianoGMP, a contract development and manufacturing organization (CDMO) specializing in oligonucleotides. The acquisition, announced in August, further differentiates its value proposition to support a broader client base across the whole oligonucleotide development continuum, from research to commercialization, EuroAPI said.
