TCR upstart gets fresh funding as it looks to charge toward the clinic – Endpoints News

2022-09-24 01:37:12 By : Ms. rebecca luo

While sev­er­al com­pa­nies have been find­ing suc­cess in the TCR-T cell ther­a­py space — with In­tel­lia hav­ing its treat­ment ac­cept­ed by the FDA last year — an­oth­er com­pa­ny is us­ing ma­chine learn­ing to get in on the ac­tion and find a can­di­date to bring to­ward the clin­ic.

Im­munoScape, a biotech based in Sin­ga­pore and Cal­i­for­nia, has raised $14 mil­lion in a fresh round of fi­nanc­ing. The com­pa­ny it­self was found­ed in 2016 as a spin­out from the Sin­ga­pore-based Agency for Sci­ence, Tech­nol­o­gy and Re­search, set­ting up its US op­er­a­tions in San Diego in 2020.

In an in­ter­view with End­points News, Im­munoScape CEO Choon-Peng Ng said the up­start is fo­cused on the dis­cov­ery and even­tu­al de­vel­op­ment of TCR-T cell ther­a­pies in the on­col­o­gy space, with a fo­cus on sol­id tu­mors. Im­munoScape us­es a ma­chine learn­ing-based tech­nol­o­gy plat­form that an­a­lyzes da­ta from its lab to in­ves­ti­gate and even­tu­al­ly de­vel­op TCR-T cell ther­a­pies.

While the com­pa­ny has not un­veiled the de­tails of its ther­a­pies just yet, Ng not­ed that it does have some tar­gets iden­ti­fied and is cen­ter­ing on treat­ments re­lat­ed to breast can­cer, prostate and lung can­cer. He said that Im­munoScape will choose its as­sets and in­sert them in­to the pipeline by the end of the year, with the biotech plan­ning to have an IND filed by 2024.

The $14 mil­lion raise will be go­ing to­ward ex­pe­dit­ing de­vel­op­ment ef­forts and get­ting a can­di­date clos­er to the clin­ic. To date, Im­munoScape has man­aged to raise $41 mil­lion in to­tal through oth­er fundrais­ing ef­forts, in­clud­ing $14 mil­lion last year. Ng said that he would not rule out any fu­ture fund­ing, and while he does rec­og­nize that the IPO can be tough to nav­i­gate cur­rent­ly, he said that the com­pa­ny will be keep­ing its eye on the mar­ket.

As for the im­me­di­ate fu­ture, Peng Ng told End­points that, apart from pur­su­ing its IND, they will al­so be hop­ing to part­ner with oth­er groups and com­pa­nies that may have an in­ter­est to de­vel­op its as­sets.

“At the end of the day, (it’s) ful­fill­ing the mis­sion in bring­ing as many of these nov­el ther­a­peu­tics to the clin­ic. And we rec­og­nize that we are a small team, and we want to do the best we can for what we can man­age,” he said.

Ng al­so not­ed that Im­munoScape is sep­a­rat­ing it­self from the pack due to its ma­chine learn­ing tech­nol­o­gy that can dis­cov­er tar­gets at scale and screen hun­dreds of epi­topes. Al­so, by dis­cov­er­ing nat­u­ral­ly oc­cur­ring TCR anti­gens, Ng be­lieves that this will give the com­pa­ny’s ther­a­pies a more pos­i­tive safe­ty pro­file.

Anzu Part­ners led the round, with Am­gen Ven­tures and Sin­ga­pore-based ED­BI al­so par­tic­i­pat­ing.

APAC is the fastest growing region globally for cell & gene therapy trials representing more than a third of all cell & gene studies globally, with China leading in the region. 

APAC is the leading location globally for CAR-T trials with China attracting ~60% of all CAR-T trials globally between 2015-2022. The number of CAR-T trials initiated by Western companies has rapidly increased in recent years (current CAGR of about 60%), with multiple targets being explored including CD19, CD20, CD22, BCMA, CD30, CD123, CD33, CD38, and CD138.

Right around the beginning of the year, we got a close-up look at what happens after a boom ripples through biotech. The crash of life sciences stocks in Q1 was heard around the world.

In the months since, we’ve seen the natural Darwinian down cycle take effect. Reverse mergers made a comeback, with more burned out shells to go public at a time IPOs and road shows are out of favor. And no doubt some of the more recent arrivals on the investing side of the business are finding greener pastures.

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Back in April, Amgen said it was encouraged by the solicitor general’s anticipated review of its Supreme Court petition to rehear a Repatha patent case. They’re likely much less optimistic about the outcome now.

Solicitor General Elizabeth Prelogar wrote in a recent 27-page brief that Amgen’s arguments “lack merit and further review is not warranted.”

The case traces back to a suit filed in 2014 against Sanofi and Regeneron’s Praluent, which ended up beating Amgen’s PCSK9 blockbuster Repatha to market by a month just a year later.

The EMA is putting EU member states on alert over the shortage of two drugs that counter heart attacks due to an uptick in demand.

On Friday, the EMA sent out a warning that two Boehringer Ingelheim drugs are experiencing a shortage: Actilyse and Metalyse. The drugs are used as emergency treatments for adults experiencing acute myocardial infarction, or a heart attack, by dissolving blood clots that have formed in the blood vessels.

At Klick Health’s first Ideas Exchange conference with biotech and pharma industry insiders since before the pandemic began, it was no surprise many conversations included Covid topics. Yet while vaccines and treatments were discussed, so too were the effects on drug development, federal responses, health inequities — and what to do now and next.

George Yancopoulos, chief scientist and cofounder of Regeneron, opened the conference responding to a question from Acorda CEO Ron Cohen about the spotlight on the industry during Covid and some of the “flak” biopharma has taken in the past.

Almost a year after the FDA gave the green light to LA-based Aadi Bioscience’s first drug, the biotech is looking to private investors to keep itself going.

The oncology player announced Thursday that it has engaged with both new and existing investors in a PIPE financing — selling 3.3 million shares at $12.50 a share, the biotech’s closing price at Nasdaq on Wednesday. The company is also selling off pre-funded warrants to purchase over 2.4 million more shares at $12.4999 per pre-funded warrant.

FDA’s outside advisors voted in favor of Ferring Pharmaceuticals’ RBX2660, an experimental poop-based drug implant that the company says would be the first microbiota-based live biotherapeutic to receive an FDA green light.

That was a point repeatedly discussed during the Vaccines and Related Biological Products Advisory Committee, or VRBPAC, meeting Thursday when evaluating Ferring’s fecal microbiota transplant, or FMT, for reducing the recurrence of Clostridioides difficile infection in adults who have received antibiotics. Multiple members brought up the need for a regulated product amid a landscape of unregulated FMTs already happening in clinical care.

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The first lab-made antibody medicine was approved in 1986 — it bound to an antigen known as CD3 on T cells and was meant to prevent kidney transplant rejection. While antibody technology improved, most antibodies were made as blocking agents, neutering clamps that attacked cells and proteins.

But then scientists got creative with their engineering. They made antibody-drug conjugates, or ADCs for short, which attached toxins or drugs to the antibodies, enabling them to kill cells. Then they made CAR-T therapies, which attached a patient’s T cell to the targeting fragment of an antibody, to destroy cancer cells.

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When Ionis and AstraZeneca unveiled the first round of mid-stage data for their antisense PCSK9 drug, Mene Pangalos, AstraZeneca’s EVP of biopharmaceuticals R&D, underscored the drug’s “potential best-in-class efficacy profile.”

But now that the second batch is in, it appears AZD8233 isn’t hitting the mark after all.

Ionis announced Friday morning that although the candidate, also dubbed ION449, met the primary endpoint in the Phase IIb SOLANO trial, its partners at AstraZeneca have decided not to move it into Phase III studies because the “results did not achieve pre-specified efficacy criteria.”

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Bioscience & Technology Business Center The University of Kansas Lawrence, Kansas

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