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Thursday, July 29, 2021

Dicerna: FDA Clears Application for Treatment of Alcohol Use Disorder

 – Novel ALDH2-Targeting GalXC™ RNAi Candidate Designed to Address a Highly Prevalent and Undertreated Disorder1 –

– Dicerna Expects to Initiate Phase 1 Clinical Trial of DCR-AUD in the Third Quarter of 2021 –

Dicerna Pharmaceuticals, Inc. (Nasdaq: DRNA) ("Company" or "Dicerna"), a leading developer of investigational ribonucleic acid interference (RNAi) therapeutics, today announced the U.S. Food and Drug Administration ("FDA") clearance of its Investigational New Drug (IND) application for DCR-AUD, the Company’s investigational RNAi candidate for the treatment of alcohol use disorder (AUD).

https://finance.yahoo.com/news/dicerna-announces-fda-clearance-investigational-113000232.html

Anavex: ANAVEX®2-73 (Blarcamesine) Significantly Prevented Aβ (Abeta)-induced Cognitive Deficits

 Pre-Treatment with ANAVEX®2-73 entirely prevented Abeta-induced cognitive decline

Anavex planning a Phase 3 prevention trial of ANAVEX®2-73 including participants at risk for cognitive and functional decline related to Alzheimer's disease

Anavex Life Sciences Corp. (“Anavex” or the “Company”) (Nasdaq: AVXL), a clinical-stage biopharmaceutical company developing differentiated therapeutics for the treatment of neurodegenerative and neurodevelopmental disorders including Alzheimer’s disease, Parkinson’s disease, Rett syndrome and other central nervous system (CNS) disorders, today reported new data that established ANAVEX®2-73 to be a preventive treatment in the pharmacological model of Alzheimer's disease (AD). Pre-treatment with ANAVEX®2-73, repeated once daily for one week before the Aβ (Abeta) challenge was protective in the Aβ25-35 peptide model of Alzheimer’s disease in mice. ANAVEX®2-73 significantly and dose-dependently prevented Aβ25-35-induced biomarker-correlated cognitive impairments, which were assessed one week after the Aβ (Abeta) insult during which no further ANAVEX®2-73 treatment took place.

https://www.globenewswire.com/news-release/2021/07/29/2271102/29248/en/Anavex-Life-Sciences-Announces-ANAVEX-2-73-Blarcamesine-Significantly-Prevented-A%CE%B2-Abeta-induced-Cognitive-Deficits-with-Confirmed-Significant-Biomarker-response-in-Animal-Model-of.html

Intercept: Ocaliva sales up 25% in Q2

 Worldwide Ocaliva® net sales of $96.6 million, representing 25% growth over the prior year quarter

Company reiterates 2021 financial guidance of Ocaliva net sales guidance of $325 million to $340 million and Non-GAAP adjusted operating expense guidance of $380 to $410 million

Updates to the Ocaliva U.S. Prescribing Information complete

Company provides regulatory update on NASH fibrosis program in the U.S.

Company to host conference call today at 8:30 a.m. ET

Conference Call on July 29, 2021 at 8:30 a.m. ET

We are hosting our second quarter 2021 financial results conference call and webcast on July 29, 2021 at 8:30 a.m. ET. The conference call will be available on the investor page of our website at http://ir.interceptpharma.com or by calling (855) 232-3919 (toll-free domestic) or (315) 625-6894 (international) passcode 2919379. A replay of the call will be available on our website shortly following the completion of the call and will be available for two weeks.

https://finance.yahoo.com/news/intercept-pharmaceuticals-reports-second-quarter-110000571.html

Annovis Bio, touting new Alzheimer's data, rips into Biogen's Aduhelm

 Eyes, money and renewed interest have poured into the Alzheimer's space in the past seven weeks following the FDA's controversial green light for Biogen's drug Aduhelm. But Annovis Bio thinks the specific interest in its company is due to data on its own AD treatment hopeful, which improves cognition by 30% in 25 days. 

The biotech said Wednesday that its oral drug, being tested in both Alzheimer's and Parkinson's disease patients, normalized biomarkers in phase 2a studies. The level of neurotoxic proteins were normalized, meaning they came down, axonal health was restored, inflammation was lowered and neurofilament light was also lowered, said CEO Maria Maccecchini, Ph.D., in an interview with Fierce Biotech. 


The data, presented Wednesday night at the 2021 Alzheimer's Association International Conference in Denver, adds to the positive results that the biotech released in May.

Improving cognition

At that time, Annovis said the drug, dubbed ANVS401, improved cognition by 4.4 points for a statistically significant improvement of 30% after 25 days, based on the Alzheimer’s Disease Assessment Scale–Cognitive Subscale 11. 

In early June, Annovis also said AD and PD patients in the phase 2a study showed a statistically significant increase of 23% to 28% in correctly coded fields after 25 days of treatment. That was based on the WAIS coding scale, which measures speed, coordination, attention, focus and accuracy, the CEO said.

Berwyn, Pennsylvania-based Annovis expects more data around synaptic markers in the coming weeks and will meet with the FDA in late-September or October to start discussing phase 3 studies, Maccecchini said. The 69-patient phase 2a study is done, with the last patient coming off on Saturday, the CEO added. 

'Even remotely as good'

Maccecchini did not mince words when describing how Annovis can compete against the recently approved Aduhelm (aducanumab), which has riddled Biogen with controversies and calls for federal investigations. 

"I don’t really feel in any way, shape or form that Aduhelm is even remotely as good as our drug. I mean, there’s just no comparison," Maccecchini said.

Aduhelm showed a 22% improvement over placebo. 

"But you have to put that in perspective. Placebo goes down 100%, and Aduhelm goes down 22% less, which means it’s 78% worse than at the beginning of the study," the CEO said. 

Annovis' drug works by restoring the information flow so that nerve cells do not die. The company has shown in animals that information flow is restored, Maccecchini said. 

"When a nerve cell gets sick, the first thing that happens to it, its information flow is sluggish. So, if the information flow is sluggish, you could understand why people think slower, forget more, walk slower, slur speech, get constipated," Maccecchini said. 

Multiple phase 3 studies

With this data in hand, and more expected in the coming months, Annovis will meet with the FDA in late September or October to consider multiple phase 3 studies in both AD and PD patients, Maccecchini said.

The company has enough money for one phase 3 study, but the CEO said she expects Annovis' stock to "go up some" and will need to raise about another $200 million to $250 million to carry out additional studies.

The biotech's stock price has skyrocketed 1,014% in the past six months. The data, however, was seen as mixed and partly confused at best from the market, which drove down Annovis' shares by nearly 36% afterhours Wednesday, and opened up in early, pre-market down more than 2%.

The phase 3 studies will enroll hundreds of patients, including a three to six month short-term study and a two-year chronic study in Alzheimer's patients, as well as one or two studies for Parkinson's patients. 

"That will really prove everything. It will prove that we can give it short-term, and it will prove that we can give it forever," Maccecchini said. 

Drug cocktail

Following phase 3 studies, Maccecchini said she thinks the drug can be studied in combination with other drugs, noting she was "just chatting" with AC Immune, which has AD and PD treatments in the clinic. 


"You know, we should combine our drugs. Every chronic condition is treated with a cocktail. Who says that using Aduhelm alone works? I mean, it works a little bit. OK, fine. But I don’t see any problem coming up with drug cocktails to make it better for different people," Maccecchini said.

The CEO said she's "really happy" with companies like Athira, Cassava, AC Immune and Anavex going after Alzheimer's "with different approaches that are combinable."

https://www.fiercebiotech.com/biotech/annovis-bio-presents-data-alzheimer-s-treatment-says-biogen-s-aduhelm-not-remotely-as-good

Wednesday, July 28, 2021

Pfizer, responding to criticism, presses case for COVID-19 booster shots

 

  • Pfizer, in a quarterly earnings presentation Wednesday, defended plans to soon seek regulatory clearance for a coronavirus booster shot, offering new details that could point to a waning effect of its shot over time.
  • The drugmaker has already butted heads with U.S. regulators about the need for a booster. But the spread of the more transmissible Delta variant and data from Israel showing potentially reduced protection from infection have raised concerns that a third shot may be necessary.
  • Presentation slides from Pfizer showed a booster elevates neutralizing antibodies against Delta, though it's unclear whether that will translate to increased protection. Still, Pfizer intends to seek emergency authorization of a booster shot as early as next month, the company said Wednesday.

The pandemic has entered a new phase because of the Delta variant, which first emerged in India and has since become the dominant strain in several countries, including the U.S.

Infections are once again rising across the globe, particularly in areas with low vaccination rates. In the U.S., Delta's spread has already led the Centers for Disease Control and Prevention to change earlier guidance about wearing masks, even for some who have been vaccinated.

Vaccinated people remain largely protected against Delta, as multiple studies have shown a two-dose regimen of Pfizer's vaccine can nearly eliminate the chance of severe illness and death from infections caused by the variant. But Pfizer has long contended a booster is needed to protect against waning immunity, and has advanced plans to test a third dose of its original shot as well as a Delta-specific vaccine.

Pfizer's assertion alarmed the Food and Drug Administration and CDC, which earlier this month issued a public rebuke and insisted that boosters aren't needed "at this time." Recent data from Israel's health ministry showing the shot was just 39% effective in preventing infections, however, appear to bolster Pfizer's case. Biden Administration health officials have reportedly begun to embrace boosters as well, at least for vulnerable groups like the elderly or immunocompromised.

During its quarterly earnings presentation on Wednesday, Pfizer advanced its case. On one slide, Pfizer showed how far neutralizing antibody levels fell against the original coronavirus strain and a different variant, Beta, over time. Levels were "quite low" eight months after the second dose, wrote Evercore ISI analyst Umer Raffat, in a note to investors.

Additionally, a preprint paper released Wednesday indicated the shot's efficacy gradually declined from 96% to 84% six months after vaccination, though it was still 97% protective against severe disease.  

"I remember saying we believed, based on the data, we will need a booster eight to 12 months from second dose," said chairman and CEO Albert Bourla, on a conference call. "We have seen with Delta we might need it a little earlier."

In another slide, Pfizer disclosed a third shot of its current vaccine drove neutralizing antibody levels against Delta more than five-fold higher for people under 55 and over 11 times higher for those older than 65 years of age. Pfizer believes that may lead to better protection than a two-shot regimen, but that hasn't been proven. The threshold for immunity isn't yet known, and there are several other immune defenders — such as B cells and T cells — involved in the body's response to infection.

Pfizer began a Phase 3 study of a third shot this month and could seek emergency clearance of a booster shot in August, the company said Wednesday. Pfizer could start a trial for a shot tailored to the Delta variant next month as well.

The company, separately, reported $7.8 billion in sales from its coronavirus vaccine this quarter and now projects more than $33 billion for the year, which would be a record for a pharmaceutical product.

An oral antiviral that Pfizer's developing for COVID-19 is in late-stage testing as well. If the results are positive, Pfizer could file for an emergency authorization by the end of the year.

https://www.biopharmadive.com/news/pfizer-coronavirus-vaccine-booster-plan-delta/604063/

Vaccines against Covid-19, venous thromboembolism, and thrombocytopenia. A population-based retrospective cohort study

 

Joan-Ramon LaporteErmengol ComaFrancesc FinaLuis Garcia-ErolesXavier VidalManuel Medina

Risk of Myocarditis from COVID-19 Infection in People Under Age 20: A Population-Based Analysis

 

Mendel E SingerIra B. TaubDavid C. Kaelber