For a biotech that opened its lab the week before the pandemic shuttered many offices, MOMA Therapeutics has experienced hardly a blip in operations, so much so that it attracted 15-year Takeda vet Asit Parikh last year as CEO and — amid a wilting financing environment — a $150 million Series B to take on the machine.
So-called molecular machines, that is. The Third Rock Ventures-incubated startup will use the proceeds to bankroll continued work on the class of enzymes that “generate force and motion within cells,” Parikh told Endpoints News.
About half of the nearly 500 enzymes in this class “have been linked to some form of disease,” the CEO said, noting some are known for unwinding DNA to aid its replication, others for degrading proteins to assist in shuttling throughout the cell.
The enzymes “grind like a work cycle, if you will,” Parikh said. Similar to the seemingly non-stop work that MOMA’s 54 employees have been putting into the startup, the CEO said.
“People started working nights and weekends. Some of our junior scientists, one of them pulled a 24-hour shift on a Sunday to keep the projects going and to keep the science moving,” the CEO said. “And it’s thanks to their hard work, but also their risk tolerance and sacrifices and just wanting to get some of this stuff done, that we are able to have a strong foundation that’s gotten us to where we are today.”
That work is geared toward MOMA’s targeted mid-2024 clinical entry, as the biotech is boosting its team by another 10 positions this year and more in 2023 to fuel three precision oncology programs, Parikh said. All three programs revolve around a common thread: DNA repair, the CEO added.
“The ideal would be yesterday, but that’s probably not going to happen now,” Parikh jokingly said of MOMA entering its first human trial.
As for the focus on oncology — out of a vast field of opportunities with molecular machines, which influences cardiovascular and respiratory diseases, immunology and other areas — MOMA decided it was the right path because of the swath of genetic cancer databases to tap into.
“The premise to understand these molecular machines at a level that nobody else does, and through the intense focus on just one class, have a benefit on human suffering from that,” Parikh said.
Now, 25 months after unveiling itself, MOMA is out with its second big round of financing to set the biotech apart from others in its native Cambridge, MA, and elsewhere in the drug development landscape. And it only took a few months for Parikh and team to gather up the funds after starting the raise in mid-January.
“The key for MOMA is to be ready for really any possible forward scenario, which is the market improves somewhat, market stays the same, or market gets even tougher than it is today, which is hard to imagine, but not inconceivable,” Parikh said. He previously helmed Takeda’s GI unit after leading Entyvio clinical studies.
Goldman Sachs led the round and was joined by other new investors Section 32, Pavilion Capital, Invus and LifeSci Venture Partners. MOMA’s entire Series A investor lineup also participated, including Third Rock, Nextech Invest, Cormorant, Casdin Capital, Rock Springs Capital, Creacion Ventures, Alexandria Venture Investments and others kept under wraps.
How are top investors navigating the longest biotech bear market in almost 20 years? RBC Capital Markets Healthcare Desk Sector Strategist Chris McCarthy discusses key fundamentals, macro-awareness and the continued impact of COVID with HealthCor’s Ben Snedeker and Omega Funds founder Otello Stampacchia.
Biotech indexes may be down, but both Snedeker and Otello Stampacchia, Ph.D., Founder and Managing Director of Omega Funds, see opportunities in the market. In Snedeker’s opinion, investors need to seek out companies with the potential for meaningful revenue growth, particularly those that are mispriced in the current bear market.
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Gout is the most common form of inflammatory arthritis, but not many people make the connection. That’s why Horizon Therapeutics is partnering with the Arthritis Foundation in a new campaign that includes outdoor murals in cities across the US. In each of the four artworks, the uric acid crystals that build up inside the body with gout are shown as bright green crystals on hands, feet or spine.
The murals include Horizon’s campaign website uncovergout.com where people can see a behind-the-scenes video about the condition and the making of the images, along with more information and patients’ stories about the stigma and misconceptions around gout.
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Three generic drugmakers have ceased operations immediately, as their holding company has enlisted a consulting firm to oversee the process of administration as 1,000 employees lose their jobs.
Doncaster Pharmaceuticals Group, Testerworld, and Eclipse Generics have brought on the consulting firm Kroll as it winds down its operations. The three wholesalers are all a part of the Converse Pharma Group, a major supplier of drugs that has more than 4,000 customers.
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Roche is ending the week with another dispiriting setback to reflect on.
Right on the heels of its big TIGIT Phase III fail, which rattled the company from top to bottom as its share price was hammered, Sandoz announced it’s rolling out the first knockoff of their blockbuster IPF drug Esbriet.
This is the first fully substitutable copy of the drug, which has been playing second fiddle to Ofev from Boehringer Ingelheim, which earned $2.7 billion last year, compared to a bit more than a billion dollars for the Roche drug. And Sandoz is doing the launch with a 0-dollar co-pay from qualified patients.
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Bristol Myers Squibb’s manufacturing facility in East Syracuse, NY, is about to be swallowed up by one of the largest conglomerates in South Korea.
Lotte Corporation and BMS unveiled a fresh deal for the site on Friday while keeping most of the details — including the financing — under wraps. BMS even declined to disclose the site’s square footage in an email to Endpoints News.
Meanwhile, South Korea’s Yonhap News Agency reported that the deal cost Lotte $160 million. In return, the conglomerate gets the site, equipment and a workforce with “technical capabilities and expertise.”
Both GlaxoSmithKline and iTeos Therapeutics are going to take a hard look at their experimental TIGIT-targeting immunotherapy in the wake of Roche’s fail earlier this week.
EOS-448, an IgG1anti-TIGIT monoclonal antibody designed to engage the Fc gamma receptor (FcγR), is being “reevaluated” by the partners, iTeos revealed in its first quarter financial report Thursday. And there may even be further delays going forward: According to an iTeos company spokesperson in an email to Endpoints News, the three registration-directed trials that were due to potentially kick off around the end of the year now will have to wait until next year.
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Checkmate Pharmaceuticals knew time was running out to fund the future of its sole asset. The cash reserves at Art Krieg’s I/O biotech would run out as the clock struck 2023, and it didn’t help that Checkmate had struggled to attract institutional investor interest in 2021 and again couldn’t eke out any semblance of acquisition appetite from five “global pharmaceutical companies.”
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After a months-long wait, UCB has finally heard back from the FDA regarding its plaque psoriasis drug. And the verdict is no.
The agency rejected the BLA for the IL-17 inhibitor, which is already approved in Europe, the UK, Japan, Canada and Australia. According to UCB, the complete response letter states that “certain pre-approval inspection observations must be resolved before approval of the application” — although it didn’t specify the problem.
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