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Tuesday, September 26, 2023

Candel: Early Survival Data From Lung Cancer Trial

 Candel Therapeutics Inc CADL announced updated activity data from its ongoing, open-label, phase 2 trial of CAN-2409 plus valacyclovir in combination with continued immune checkpoint inhibitor (ICI) treatment in patients with non-resectable, stage III/IV non-small cell lung cancer (NSCLC), who have an inadequate response to front line anti-PD(L)1 therapy

These patients historically have had an expected median overall survival of 10-13 months. 

The aim of the CAN-2409 immunotherapy antitumor strategy is to raise the tail on the survival curve by increasing the number of long survivors beyond 10-13 months.

Of the 40 evaluable patients, 15 have lived ≥ 12 months; of these, 10 patients have lived > 18 months, of whom 70% (7/10) were alive as of the last follow-up. 

All four patients (100%) with OS > 24 months were alive at the last follow-up, with the longest reaching 31.7 months.

An additional 18 out of the 40 evaluable patients are also alive but have not yet reached 12 months of follow-up.

Candel continued to observe a favorable safety/tolerability profile after CAN-2409 treatment.

Candel expects to share topline overall survival data for Cohort 2 in the second quarter of 2024, assuming mature data then.

https://www.benzinga.com/general/biotech/23/09/34915228/candel-therapeutics-reveals-early-survival-data-from-lung-cancer-trial

Takeda Puts Nearly $600M on the Line for AcuraStem’s ALS Program

 Takeda on Monday inked a development and commercialization agreement with California-based biotech AcuraStem to target amyotrophic lateral sclerosis and other neurodegenerative diseases.

Under the terms of the deal, Takeda will pledge upfront and milestone payments of up to approximately $580 million if the collaboration meets all future clinical, regulatory and commercial milestones. AcuraStem will also be eligible to receive tiered royalties on potential net sales of any product that emerges from the partnership.

In return, the Japanese multinational pharma will gain access to AcuraStem’s PIKFYVE program, which includes AS-202, an investigational antisense oligonucleotide (ASO) and the biotech’s most mature candidate. Takeda will have exclusive worldwide license to AS-202 as well as to AcuraStem’s other PIKFYVE-directed assets.

AcuraStem will take charge of certain studies to enable an Investigational New Drug application for AS-202, while Takeda will be responsible for all development activities, including clinical studies, regulatory efforts and commercialization, according to the announcement.

PIKFYVE is an emerging therapeutic target in amyotrophic lateral sclerosis (ALS), according to AcuraStem’s website. The company’s studies have shown that using an ASO therapeutic to inhibit the gene that encodes for the kinase helps neurons discard toxic proteins and pathologic aggregates. In turn, this restores healthy neuron function and prevents neurodegeneration.

This mechanism of action also points to the potential of AcuraStem’s PIKFYVE approach to frontotemporal dementia (FTD) and other diseases caused by the misfolding, and eventual clumping, of the protein TDP-43.

In many pre-clinical models of ALS and FTD, using PIKFYVE-targeted ASOs, such as AS-202, can reverse the pathological protein deposition in neurons, according to AcuraStem.

In a statement, Sarah Sheikh, head of Takeda’s Neuroscience Therapeutic Area Unit, said that “through its unique dual mechanism of action, which addresses TDP-43 aggregation and improves TDP-43 function,” AS-202 has the potential to address the existing unmet need among patients with “debilitating neurological diseases.”

Takeda has also inked other high-value deals this year. In July 2023, the company signed a strategic discovery collaboration and licensing agreement with British biotech F-star Therapeutics to discover next-generation and multi-specific antibodies for cancer targets. Though the complete financial details of the deal were not revealed, the companies said that F-star could receive up to $1 billion in milestones.

In January, Takeda entered into another potential billion-dollar deal with Hutchmed to develop fruquintinib, a VEGF inhibitor being trialed for colorectal cancer.

https://www.biospace.com/article/takeda-puts-nearly-600m-on-the-line-for-acurastem-s-als-program/

EU in talks with Moderna over new deal for COVID vaccines

 The European Union is in talks with Moderna over a new supply deal for the company's COVID-19 vaccines amid concerns over a rise in infections in the region, the Financial Times reported on Tuesday, citing two people familiar with the matter.

The company supplied its COVID vaccines to the EU during the pandemic, but the contract for its Omicron-adjusted vaccines ended in August last year and was not renewed.

At least eight countries in the union are interested in a new supply deal, the report said, citing one of the people.

"Moderna manufactured its updated COVID-19 vaccine at risk to ensure we could support member states with their upcoming vaccination campaigns," a company spokesperson said, adding the updated shot was approved in Europe and ready to be supplied.

Updated COVID shots that will be used in the vaccination campaign this year will target the XBB.1.5 variant of Omicron.

The spokesperson said an agreement with the European Commission is the fastest way to procure the shots, which would help ensure a diversified supply of COVID vaccines with vaccination campaigns set to start in October.

A spokesperson for the European Commission declined to comment on the talks over Moderna's supply contract, but added it "has been assessing the needs and interests of the Member States for additional COVID-19 vaccines".

Currently, Pfizer and its German partner BioNTech's updated COVID shot is the most widely used vaccine in the region.

Pfizer and BioNTech in May reached a deal to amend their COVID-19 vaccine contract by cutting the number of shots the EU must buy and pushing the delivery deadline to 2026 due to gradually falling demand for the shots

https://finance.yahoo.com/news/1-eu-talks-moderna-over-123334736.html

Ionis' metabolic disorder drug lowers high levels of a type of fat in study

 Ionis Pharmaceuticals said on Tuesday its experimental drug met the main goal of reducing abnormally high levels of the most common type of body fat in a late-stage trial in patients with a metabolic disorder.

The rare genetic disorder, known as familial chylomicronemia syndrome (FCS), prevents the body from breaking down fats and is characterized by extremely high levels of triglyceride.

FCS is caused by the deficiency or impaired function of lipoprotein lipase enzyme, responsible for breaking down triglycerides, which when accumulated in the blood leads to inflammation of the pancreas.

The National Pancreas Foundation estimates FCS to occur in 1 in 1-2 million people globally.

The drug candidate, olezarsen, showed statistically significant reduction in levels of triglyceride compared to placebo, as well as showed a 100% reduction in inflammation of the pancreas, Ionis said.

The company said it plans to file a marketing application with the U.S. Food and Drug Administration for olezarsen early next year.

Shares of the California-based drug developer rose 3% to $44 in premarket trading.

If approved, olezarsen will be the first available treatment for FCS in the U.S., Ionis said.

https://finance.yahoo.com/news/1-ionis-pharmas-genetic-disorder-112807957.html

Bullfrog: Positive Data from Preclinical Study for Treatment of Glioblastoma

  BullFrog AI Holdings, Inc. (NASDAQ: BFRG; BFRGW) ("BullFrog AI" or the "Company"), a technology-enabled drug development company using artificial intelligence (AI) and machine learning to enable the successful development of pharmaceuticals and biologics, today announced positive data in a preclinical study investigating the anti-cancer activity of a novel prodrug of mebendazole for the treatment of glioblastoma. The study assessed the relative efficacy of BF-222, a novel formulation of mebendazole that has been evaluated in clinical trials, and BF-223, a novel prodrug of mebendazole with improved solubility and bioavailability relative to BF-222, compared with placebo in mice that had been implanted with tumor cells as a model for human glioblastoma.

Animals treated with BF-223 had an average survival time of 27.9 days compared with 27.3 days for mice treated with BF-222 and 23.4 days for mice given placebo. Mice treated with BF-223 were administered 80% of the dose that mice treated with BF-222 received, and improved outcomes for both treatment groups were statistically significant compared to placebo. In addition, animals treated with equivalent doses of BF-222 and BF-223 showed comparable and significant reduction in tumor growth compared to control animals during the study.

https://finance.yahoo.com/news/bullfrog-ai-announces-positive-data-120000742.html

Italy's Alfasigma to buy US liver disease drugmaker Intercept for nearly $800 mln

 Italy's Alfasigma S.p.A agreed on Tuesday to buy drugmaker Intercept Pharmaceuticals for $794 million as it aims to expand its treatment portfolio in liver diseases and digestive system disorders, and bolster presence in the U.S.

The proposed all-cash acquisition would add Intercept's Ocaliva, a treatment for liver disease primary biliary cholangitis, to Alfasigma's portfolio.

Morristown, New Jersey-based Intercept forecasts sales of $320 million to $340 million from the drug this year.

Alfasigma's acquisition of Intercept and its drug Ocaliva makes "best economic cost sense" given that a larger company can market and commercialize the drug with better margins and scale than a smaller biotech, Jefferies analyst Michael Yee said.

The deal comes after Intercept dropped out of the race to develop the first treatment for patients with non-alcoholic steatohepatitis (NASH), a liver disease that affects 5% of U.S. adults, after the U.S. health regulator declined to approve its drug in June.

Following this, Intercept discontinued all NASH-related investments, reduced about one-third of its workforce and restructured its operations to strengthen focus on rare and serious liver diseases.

Alfasigma will pay $19 per Intercept share, which represents a premium of 82% to its last closing price. Intercept's stock surged 77.54% to $18.53 in morning trading on Tuesday, but has fallen 15.6% this year alone. Its shares are down significantly from their peak of roughly $445 in 2014.

The deal is expected to close by the end of the year.

Alfasigma is among Italy's biggest pharmaceutical groups, with its portfolio ranging from prescription drugs to nutraceuticals. Its over-the-counter products include Biochetase, Neo-Borocillin, Dicloreum and Yovis. 

https://finance.yahoo.com/news/1-italys-alfasigma-buy-drugmaker-122728481.html

Soleno: Significant Top-line Results from Study C602 of DCCR for Prader-Willi

 Study Met Primary Endpoint; Highly Statistically Significant Difference in Change from Baseline in HQ-CT Total Score for DCCR Compared to Placebo (p=0.0022)

Soleno Intends to Submit a New Drug Application for DCCR in PWS Mid-Year 2024

Company to Host Conference Call and Webcast Today at 9:00 AM ET

Conference Call and Webcast Details
Soleno will host a conference call and webcast to discuss these results today, September 26, 2023 at 9:00 AM ET. Details can be found below:

Title:

Randomized Withdrawal Period of Study C602 Top-line Results

Date:

Tuesday, September 26, 2023

Time:

9:00 AM ET

Conference Call Details:

Toll-free: 1-877-423-9813
International: 1-201-689-8573
Conference ID: 13741535

Call me™ Feature (avoid waiting for operator):

Click Here

Webcast:

Webcast Link – Click here


A replay of the call will be available following the call on the Investors section of the Soleno website.

https://finance.yahoo.com/news/soleno-therapeutics-announces-positive-statistically-113000169.html