AnHeart Therapeutics co-founder and CEO Jerry Wang (L); co-founder and CBO Lihua Zheng (R)
In China, the character 安, pronounced An in English phonics, has a few different translations — yet they all come to the same general meaning: calm, safe, comfortable.
And for precision oncology biotech AnHeart Therapeutics, that Chinese character helps to define the company’s objective.
‘In Chinese, the pronunciation actually means something — [it] has special meaning: calm, safe, comfortable. So it’s really — you have a very calm heart, comfortable heart full of patients. So we try to make medicine so the patient can feel comfortable, feel safe. Feel calm,’ AnHeart CBO and co-founder Lihua Zheng told Endpoints News.
The low profile, Chinese-New York biotech announced this morning that it has finished an oversubscribed Series B — netting $61 million in its largest raise to date. The round, led by new investor Octagon Capital, tagged a few other investors in the financing, including Eli Lilly-linked Innovent, SagePartners and Laurion Capital. This new raise brings AnHeart to a total raise of $100 million since its inception — but that cash flow won’t last the biotech too long. The company has expanded significantly since January, going from 27 employees across its offices in China and New York in January to 65 employees as of Monday.
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With current plans to expand the company to 100 employees next year, the $61 million is only slated to last AnHeart 12-18 months, Zheng said. And AnHeart will start looking to fill a Series C sometime in Q2 next year.
The biotech, founded in December 2018 after in-licensing their three current drug candidates from Daiichi Sankyo — retaining global rights for two of the candidates and ex-Japan rights for the third — has a current lead candidate known as taletrectinib, a combination ROS1 and NTRK inhibitor that is in Phase II trials for NSCLC. According to Zheng, the Phase II trials can be considered registrational as the potential population to study with certain mutated NSCLC may be too limited for Phase III research.
And for Zheng, what makes taletrectinib unique is that for patients with ROS1 mutations in their cancer, the drug can overcome physical resistance to crizotinib, an earlier-generation NSCLC treatment that targets primarily ALK mutations, with a minor focus on ROS1 mutations. And that physical resistance in patients with mutated-NSCLC has been documented and studied over the last decade.
For drug approval, while Zheng did not provide specifics, he did say that the general timeline is it expects to file an NDA in China sometime in Q2 or Q3 next year — with the US being a year after that.
And regarding any plans to expand AnHeart’s pipeline beyond the three current candidates, AnHeart has started development on some in-house programs, but those targets remain undisclosed.
Sensor-based technology for clinical trial data collection represents the latest medical paradigm shift. There are more than 700 clinical studies involving wearable devices currently underway in the United States. A study from Intel IT projects their inclusion in clinical trials will surge to 70% by 2025.
Apps, biosensors and patient-centered technologies increase visibility of comprehensive patient data. Pharma leaders anticipate the benefits of wearables to include better data (58%), faster results (33%) and lower trial costs (10%).
When Bristol Myers Squibb celebrated the approval of ozanimod — branded Zeposia — in ulcerative colitis earlier this year, the company touted the first gastrointestinal indication for an S1P receptor modulator.
Now Pfizer wants to give the pharma rival a run for its money.
Pfizer is dropping $6.7 billion to acquire Arena Pharmaceuticals, whose lead drug, etrasimod, targets the sphingosine 1-phosphate receptor.
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Sen. Ron Wyden (D-OR) (Graeme Sloan/Sipa via AP Images)
It’s no longer a secret that the US government is going to have to pay for Biogen’s new and expensive Alzheimer’s drug Aduhelm on the backs of huge increases in Medicare premiums.
CMS explained last month that Medicare Part B will have to increase (by the largest amount ever) its standard monthly premium — from $148.50 in 2021 to $170.10 in 2022 — in part because of the massive spending that could occur should CMS sign off on a national coverage decision for Aduhelm, and its $56,000 annual price tag next year.
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Harpreet Singh, Immatics CEO (Credit: Allogeneic Cell Therapies Summit)
Just a few weeks after offering a positive readout on its first early clinical-stage offering, the transatlantic biotech Immatics is back with news that the research crowd around Rupert Vessey at Bristol Myers Squibb has anted up $150 million in cash to get on at the ground floor with one of their still-preclinical efforts.
This time the news is centered on IMA401, Immatics’ most advanced bispecific, which uses one binder to latch on to MAGEA4/8 while another is used to whip up T cell activity against tumor cells where that’s a common antigen. For now, that’s still a preclinical effort, with the first human trial set to launch in the first half of next year.
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Australia’s CSL is plopping down $11.7 billion to acquire Vifor Pharma, the Swiss biotech best known for its iron products and kidney drugs.
While the buyout comes as little surprise — rumors have swirled since early December, and Vifor actually confirmed the deal talks to media on Monday — the final price could raise some eyebrows.
At $179.25 per share, CSL’s offer comes in much higher than the ‘more than $8.5 billion’ price tag cited in reports.
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Albert Bourla, Pfizer CEO (Getty Images)
A new private study by South Africa’s largest insurer, Discovery Health, suggests that Pfizer and BioNTech’s Covid-19 vaccine is just 33% effective against infections by the Omicron variant.
However, the variant appears to cause less severe disease, the company reported. The data, based on 211,000 positive Covid cases, showed that risk of hospitalization was 29% lower than in South Africa’s first wave back in mid-2020.
The current generation of cell therapies has proven a game changer in terms of treating aggressive blood cancers, but the tech has its limitations. Novartis, one of the biggies in the current generation of these drugs, is now taking lessons learned from CAR-T Kymriah to supercharge a ‘second-generation’ of CAR-Ts putting superior cells into patients faster.
Novartis on Monday rolled out early Phase I data for a pair of autologous CAR-T cell therapies developed through the drugmaker’s T-Charge platform, a process designed to promote T cell ‘stemness’ — a measure of a cell’s ability to self-renew — by cutting manufacturing times and spurring cell proliferation primarily in patients’ lymph nodes.
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Rumors have swirled around a potential buyout of Switzerland’s Vifor Pharma by Australia’s CSL since the start of December, and now the gossip reportedly has some truth to it.
Vifor confirmed to Reuters early Monday that it is in discussions to be acquired by CSL for more than $8.5 billion, sending its shares up more than 15% in overseas trading. The deal is expected to be finalized Tuesday, according to Australian media, with one large investor reportedly willing to pay more than $173 per share — about $60 more than Vifor’s price before the rumors began circulating on Dec. 2.
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Soon after San Francisco-based Genentech won an EUA for tocilizumab as a treatment for hospitalized Covid patients last summer, the company announced a shortage of the drug while pointing to the emergence of the Delta variant and the slowing of vaccination rates across the US.
‘This new wave of the pandemic has led to Genentech experiencing an unprecedented demand for Actemra IV– well-over 400% of pre-COVID levels over the last two weeks alone and it continues to increase,’ the company said in August.
https://endpts.com/lining-up-a-filing-for-lead-ros1-inhibitor-transpacific-oncology-biotech-anheart-therapeutics-raises-61m/