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Wednesday, October 19, 2022

Advaxis and Ayala Merge to Home In on Desmoid Tumors, Prostate Cancer

 Advaxis and Ayala Pharmaceuticals announced Wednesday they have entered into a reverse merger deal to focus on two clinical-stage cancer therapies: AL102 for desmoid tumors and ADXS-504 for prostate cancer.

In a conference call, Kenneth A. Berlin, president and CEO of Advaxis, said that Advaxis had been looking for a deal with a clinical-stage asset, and after the merger, they will “have $20 million in cash and a highly skilled team.” 

The companies will reprioritize the pipeline and focus on Wilmington, Delaware-based Ayala’s lead asset, AL102, which is currently in a Phase II/III RINGSIDE trial in desmoid tumors. They have also seen promising interim data from the trial with tumor shrinkage in the majority of patients that appears to be deepening over time.

AL102 has received Fast Track Designation from the FDA.

Roni Mamluk, Ph.D., president and CEO of Ayala, referred to the interim data presented in Sept. 2022 as having a “very intriguing therapeutic index,” adding that, “altogether the early data was considered promising … for the treatment of desmoid tumors.”

Desmoid tumors are noncancerous growths in the connective tissue. They tend to be a disease of the young, affecting people between the ages of 15 and 60. They are more common in females than males. Although benign, they can be very painful and are difficult to completely remove with surgery. According to the National Cancer Institute, two to four people out of every one million worldwide are diagnosed each year.

The companies will continue working on another Ayala compound, AL101, being developed for recurrent/metastatic adenoid cystic carcinoma.

The company is expecting a data readout on Rehovot, Israel-based Ayala, ADXS-504 in 2023, with additional data readouts for AL102.

A "Truly Transformational Deal"

Berlin said the merger offered “a number of big opportunities to advance Advaxis to a clinical-stage company.” He added it would be a “stronger oncology company with a strong pipeline and a global presence” in a “better position to trade on the Nasdaq.”

Mamluk noted that “the rationale for the merger for Ayalas is very clear — we were looking to advance our clinical programs and strengthen our U.S. presence. This merger accomplishes both goals.”

Berlin will remain president, CEO and director of the merged company. Andres Gutierrez, M.D., Ph.D., current CMO of Advaxis, will continue in that role, and Igor Gitelman, will remain Interim CFO.

Mamluk and Yossi Maim, CFO of Ayala, will both resign and assist with the transition. Gary Gordon, M.D, CMO of Ayala, is also stepping down, but plans to remain in an advisory role for some time. 

The board of directors of the merged companies will consist of seven members, two from Advaxis, four designated by Ayala, and Berlin. They intend to keep operations in Israel, where most of the Ayala team is based.

Ayala shareholders will own 62.5% of the combined company’s outstanding common stock. Advaxis stockholders will own about 37.5%. 

Berlin described the merger as a “truly transformational deal “with “near-term commercial potential.”

He added that they see AL102 as having the “potential to have a competitive advantage and a decent place for the compound in the commercial market.

Although “cash is a critical component to the deal, it’s not the whole picture,” Berlin noted. They expect “some key milestones in 2023, and we believe we can modulate spending if needed in a tough capital market and not unduly delay the A102 program if we do.”

https://www.biospace.com/article/advaxis-and-ayala-merge-to-focus-on-clinical-stage-rare-and-aggressive-cancers/

Jazz Drops $50M for Exclusive Rights to Zymeworks’ Bispecific HER2 Hopeful

 Jazz Pharmaceuticals and Zymeworks Inc entered into a $50 million licensing agreement over zanidatamab, Zymeworks’ bispecific antibody targeting HER2, the companies announced Wednesday.

The deal will give Jazz exclusive commercialization and development rights over zanidatamab in the U.S., Europe, Japan and all other territories that aren’t yet covered by existing licenses. Aside from the $50 million upfront payment, Jazz is putting $325 million more on the line if it decides to continue the collaboration.

This will be decided once topline data from the HERIZON-BTC-01 trial comes in, which is expected to happen before the year ends.

Zymeworks will also continue to be eligible for $524 million in certain regulatory milestones and up to $862.5 million in commercial milestones, bringing the overall potential value of the deal to $1.76 billion. Zymeworks can earn 10% to 20% of tiered royalties on net sales.

The companies expect to close the deal by the end of the year.

“This transaction enables Zymeworks to leverage Jazz’s existing integrated capabilities and global infrastructure to commercialize efficiently,” Kenneth Galbraith, chair and CEO of Zymeworks said in an investor call Wednesday morning. 

“This agreement creates significant value for Zymeworks and its stockholders and fulfills a major strategic objective we identified in January of this year of identifying and enacting a global partnering transaction for zanidatamab within this calendar year,” he added.

A New Addition to an Expanding Oncology Pipeline

Discovered through Zymeworks’ proprietary Azymetric platform, zanidatamab is a bispecific antibody that targets two non-overlapping epitopes on the HERT2 protein, a central molecule in many different cancers.

This molecule design gives zanidatamab novel mechanisms of action against cancer. For instance, it can induce a dual blockade of the HER2 signaling pathway and achieve a more thorough removal of the HER2 protein from the surface of the tumor cell.

Zanidatamab has shown strong anti-tumor activity against different HER2-expressing cancers, both when given as a standalone therapy or in combination with other agents. 

The bispecific candidate is currently being evaluated as a second-line treatment option in biliary tract cancer. The FDA has granted zanidatamab Breakthrough Therapy designation, underlining its first-in-class potential in this indication.

The candidate is also being tested as frontline therapy in gastroesophageal carcinoma, for which zanidatamab, in combination with chemotherapy, has the potential to be a best-in-class intervention.

The agreement with Zymeworks aligns with Jazz’s push to expand its oncology pipeline. In April, the Irish biotech entered into a similar licensing deal with Werewolf Therapeutics, paying $15 million for exclusive global development and commercialization rights to WTX-613. A preclinical engineered IFN⍺2b cytokine pro-drug, WTX-613, marked Jazz’s first foray into immuno-oncology.

“Once we see the data from the BTC trial, we will be better positioned to provide more information, but we see this deal as likely to generate revenue in 2025,” Rob Iannone, M.D., M.S.C.E., executive vice president and global head of research and development at Jazz, told BioSpace. “Importantly, this transaction is a key part of positioning us for future growth even beyond Vision 2025, bolstering our pipeline and further diversifying our revenue stream.”

Zanidatamab joins Jazz’s robust pipeline of late-stage cancer assets, including lurbinectedin for small cell lung cancer and JZP351 for acute myeloid leukemia. Both are in Phase III studies.

https://www.biospace.com/article/jazz-drops-50m-for-exclusive-rights-to-zymeworks-bispecific-her2-hopeful/

RedHill Granted New COVID-19 Treatment Patent

 USPTO grants new method of use patent for the inhibition of a disease caused by a coronavirus in patients having pneumonia and receiving supplemental oxygen at a fraction of inspired oxygen (FiO2) up to and including 60%

Previous variant-agnostic efficacy data for opaganib, an investigational new drug for COVID-19 disease and several other viral diseases, highlights its promising profile as a broad acting, host-directed candidate therapy for pandemic preparedness

Development of opaganib for moderately severe COVID-19 patients is ongoing, including ongoing and planned pandemic preparedness research collaborations with US governmental agencies, pivotal Phase 3 trial design and regulatory clearances, and securing of external non-dilutive funding

https://finance.yahoo.com/news/redhills-oral-broad-acting-antiviral-110000597.html

Veeva upped to Neutral from Underweight by JPMorgan

Target to $170 from $225

https://finviz.com/quote.ashx?t=VEEV&ty=c&ta=1&p=d

Moderna: Omicron BA.1-Targeting Bivalent Vaccine Shows Superior Antibody Response as 4th Booster

 Data indicate durable immune response from bivalent booster after three months of follow-up

mRNA-1273.214 also demonstrated potent response to Omicron BA.2.75

 Moderna, Inc., (NASDAQ:MRNA) a biotechnology company pioneering messenger RNA (mRNA) therapeutics and vaccines, today announced new clinical data on its bivalent Omicron-containing booster, mRNA-1273.214. Ninety days after administration as a fourth booster dose in previously vaccinated and boosted participants, a 50 µg booster dose of mRNA-1273.214 elicited a superior neutralizing antibody response against Omicron BA.1 when compared to a 50 µg booster dose of mRNA-1273 in all participants regardless of prior infection. Superior performance against Omicron BA.1 was also durable, with higher antibody titers sustained through three months.

In addition, mRNA-1273.214 demonstrated significantly higher neutralizing antibody responses against Omicron BA.4/BA.5 compared to mRNA-1273 28 days after administration, as previously reported. Potent responses were also seen against Omicron BA.2.75 28 days after administration, suggesting that the bivalent booster elicits broad cross-neutralization against Omicron variants.

"Our bivalent boosters continue to demonstrate a strong, enduring response to COVID-19 variants of concern," said Stéphane Bancel, Chief Executive Officer of Moderna. "Clinical trial data now indicates that the superior immune response produced by our bivalent booster has durability for at least three months. As COVID-19 remains a global threat and a leading cause of death globally, this is an encouraging development, showing that a bivalent booster dose will offer important protection leading into the winter months."

Observed side effects of mRNA-1273.214 were similar or less severe than those of either a second or third dose of the original vaccine. Additionally, no new safety concerns were identified in the three-month follow-up.

Xenon started at Outperform by Raymond James

 Target $52

https://finviz.com/quote.ashx?t=XENE&ty=c&ta=1&p=d

IceCure Eyes Proceeding with System for Early Low-Risk Breast Cancer with High Risk to Surgery

 

  • 43,000 cases estimated annually in the U.S. alone for indication in initial filing representing an estimated $80 million annual addressable market  

  • 65,000 cases estimated annually in the U.S. for broader indication Company intends to file based on FDA's guidance, reflecting the full ICE3 study population after ICE3 5-year follow-ups are completed for all patients in 2024

  • To date, the Ipsilateral Breast Tumor Recurrence (IBTR) rate for the entire study population is 3.09%

  • Submission data include IBTR as the primary endpoint