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Monday, June 14, 2021

Enochian Bio: FDA Acceptns "Pre-IND Request For Potential HIV Cure'

 Enochian BioSciences, Inc., a company focused on gene-modified cellular and immune therapies in infectious diseases and cancer, today announced that the FDA has accepted a Pre-IND (Investigational New Drug) request for a potential functional cure or treatment of HIV. Written comments are expected this Fall.

Dr. Serhat Gumrukçu, co-founder and inventor of Enochian BioSciences, and Director of Seraph Research Institute (SRI), submitted the Pre-IND. The request was based on the results of a 54-year old man living with HIV who had failed to suppress the virus with antiviral therapy. The patient subsequently achieved viral control for 255 days with an innovative treatment of Natural Killer (NK) and Gamma Delta T-cells (GDT) collected from another person. During the entire period, no antiviral drugs were given. It is believed that the GDT cells, a small subset of immune cells that can be infected with HIV, could be a key factor in controlling the virus.

The findings were presented during the Conference of the American Society of Gene and Cell Therapy this past May. Presentations can be found at Enochianbio.com/Collaborations

Enochian BioSciences holds the exclusive license for the proprietary technology.

This innovative cellular therapy could be an important approach to achieve a “functional cure” of HIV, potentially allowing persons with the virus to stop antiviral treatment for extended periods of time. The Pre-IND submission requested that the novel strategy be extended to persons with HIV who have achieved suppression of the virus with antiviral treatment.

https://finance.yahoo.com/news/enochian-biosciences-announces-fda-acceptance-110000386.html

Synthetic biology solutions provider Codex DNA files for a $100 million IPO

 Codex DNA, which makes an automated synthetic biology workstation and related solutions, filed on Friday with the SEC to raise up to $100 million in an initial public offering.


Codex DNA states that its synthetic biology solution addresses the bottlenecks across the multi-step process of building DNA and mRNA. A key part of its solution is its BioXp system, an end-to-end automated workstation that fits on the benchtop and provides ease-of-use and hands-free automation. The company commercially launched its current synthetic biology solution in September 2019, which now includes the BioXp 3250 system, BioXp kits with associated cloud-based application scripts, and benchtop reagent kits.

The San Diego, CA-based company was founded in 2011 and booked $8 million in sales for the 12 months ended March 31, 2021. It plans to list on the Nasdaq under the symbol DNAY. Codex DNA filed confidentially on March 16, 2021. Jefferies, Cowen, and KeyBanc Capital Markets are the joint bookrunners on the deal. No pricing terms were disclosed.

Retinal Tissue Restored in Patients with Dry AMD, Heralding Paradigm Shift

 Retinal tissue has been regrown in three patients with age-related macular degeneration (AMD) with geographic atrophy or dry (atrophic) AMD in a Phase I/IIa study conducted by Lineage Cell Therapeutics.

“This has the potential to offer a whole new paradigm to treat the disease,” Brian Culley, CEO of Lineage, told BioSpace.

Adding to the original findings reported last year, two additional patients treated in November demonstrated a reduction in atrophied retinal tissue, making them – to the company’s knowledge – the only patients with dry AMD to actually regrow retinal tissue and improve visual acuity.

The treatment, OpRegen®, is an allogeneic retinal pigment epithelium (RPE) cell transplant therapy. In a 12-person study of dry AMD patients who retained some vision, 83% reported the vision in the treated eye was at or above baseline. Coincidentally, the same percentage reported that vision in their untreated eye worsened. So, although OpRegen® doesn’t reverse blindness, by causing tissue to regrow, it may be able to prevent people with dry AMD from worsening and eventually becoming blind.

In the study, RPE atrophy was measured using clinical high-resolution optical coherence tomography (OCT). It showed new areas of RPE monolayer with overlying ellipsoid zone, external limiting membrane, and outer nuclear layer that were not present during the baseline assessment. Visual acuity likewise increased.

These findings suggest the new RPE cells integrated with functional photoreceptors in areas that previously lacked those cells. The effects were most prominent in the transitional area around the primary area of geographic atrophy. Taken all together, they support the notion that atrophic AMD is reversible and that some portion of the diseased retinal tissue can be recovered.

OpRegen® is composed of functional retinal pigment epithelia (RPE) cells that Lineage manufactures by the billions from a single cell line and transplants into the eye via pars plana vitrectomy as part of a 30-minute surgery using local anesthesia.

“When we place the cells in the subretinal space, they clear the waste material and support the surrounding tissues. There also may be some degree of trophic, or nourishing, effect on nearby cells,” Culley said.

The therapy was administered as a one-time treatment and cells have persisted in the earliest-treated patients for more than five years.

Lineage plans to follow the patients for six months and then design another clinical study with input from the FDA to enable a regulatory filing market authorization.

“We believe the next trial could be a registrational study,” he said.

“Dry AMD is a progressive degenerative condition. It’s a one-way street,” Culley said. “Dry AMD cannot be reversed and has no FDA-approved treatments.”

There are a few efforts to prevent the area of atrophy from expanding, but no therapies – save OpRegen – have shown the ability to reverse the damage. Lineage Cell Therapy’s data is early, he admitted, but reiterated that the therapy appears to be capable of reversing the damage.

“Human beings cannot regrow retinal tissue, so we believe our transplanted RPE cells are responsible for these positive changes”, Culley said.

The improvements in vision are not just significant for surgeons, but are also meaningful to patients. Importantly, the benefits observed in the retinal restoration patients have been maintained for as long as three years – the duration (so far) of the longest available follow-up.

“That’s not what normally happens in dry AMD,” Culley said. Because the disease is progressive and degenerative, “A treatment that even could stabilize the disease would be a tremendous success,” so a therapy that reverses the disease could be life-changing.

Life-changing” is, in fact what one of the patients called it. “She called her physician, literally crying for joy,” Culley said, recounting a conversation with one of the principal investigators. “He said he’s never had that happen with patients who had dry AMD.”

This therapy is based on a long-hypothesized idea “that in atrophic AMD patients, cells in the transition areas at the boundaries of the geographic atrophy are dysfunctional and dying, but not completely lost  Jordi Monés, M.D., Ph.D., director, Institut de la Màcula, and director, principal investigator and founder, Barcelona Macula Foundation,  said in an earlier statement.

Now, Monés continued, “These unprecedented findings provide further evidence that the addition of new RPE cells may restore the microenvironment of the surrounding tissue and contribute to the survival and function of existing cells that otherwise, if left untreated, would inevitably progress to further expansion of the atrophic region.”

Lineage is patenting the technology internationally under the Patent Cooperation Treaty, which enables a company to seek patent protection in the 150-PCT signatory countries by filing one patent application. By filing under the PCT, the allowed claims of national patents based on the PCT application would have an estimated expiration date no earlier than May 24, 2041, which is somewhat longer than those filed one country at a time. 

“The production methods that create our cells cannot be replicated by competitors, but it’s prudent to take a belt and suspenders approach and also protect our materials and manufacturing methods with traditional patents,” Culley said.

https://www.biospace.com/article/retinal-tissue-restored-in-patients-with-dry-amd-heralding-paradigm-shift/

Gilead Longer Data for Kite's Yescarta® inFollicular Lymphoma Shows Substantial Survival Improvement

 94% of Patients Achieved a Response at 18 Months in Pivotal ZUMA-5 Trial --

-- Yescarta Reduced Risk of Death by 58% Compared to Current Therapies in Weighted Analysis of ZUMA-5 Compared to SCHOLAR-5 External Control Cohort --

-- Late-breaking Data Presented at European Hematology Association (EHA) 2021 --

https://www.marketscreener.com/quote/stock/GILEAD-SCIENCES-INC-4876/news/Gilead-Sciences-nbsp-Longer-term-Data-for-Kite-s-Yescarta-in-Relapsed-or-Refractory-Follicular-Ly-35587447/

Novavax COVID-19 Vaccine Shows 90% Overall Efficacy, 100% Protection v. Moderate, Severe Disease in Phase 3

 

  • 93% efficacy against predominantly circulating Variants of Concern and Variants of Interest
  • 91% efficacy in high-risk populations
  • 100% efficacy against variants "not considered Variants of Concern/Interest"
  • All COVID-19 hospitalizations/death occurred in the placebo group
  • Company to host investor conference call today at 8:30 am ET

Conference Call

Novavax will host a conference call today at 8:30am ET. The dial-in numbers for the conference call are (866) 652-5200 (Domestic) or (412) 317-6060 (International). Participants will be prompted to request to join the Novavax, Inc. call. A replay of the conference call will be available starting at 7:30 p.m. ET on June 14, 2021, until 11:59 p.m. ET on June 21, 2021. To access the replay by telephone, dial (877) 344-7529 (Domestic) or (412) 317-0088 (International) and use passcode 10157478.

A webcast of the conference call can also be accessed on the Novavax website at novavax.com/events. A replay of the webcast will be available on the Novavax website until September 14, 2021.

https://www.biospace.com/article/releases/novavax-covid-19-vaccine-demonstrates-90-percent-overall-efficacy-and-100-percent-protection-against-moderate-and-severe-disease-in-prevent-19-phase-3-trial/

Celltrion: Positive top-line results in Phase III trial of regdanvimab anti-COVID-19 monoclonal antibody

 

  • Regdanvimab (CT-P59) (40mg/kg) achieved statistically significant and clinically meaningful results in four main endpoints including primary and three key secondary endpoints; the company anticipates full Phase III data to be released in the coming months
  • Regdanvimab (CT-P59) significantly reduced the risk of COVID-19 related hospitalisation or death by 72% for patients at high- risk of progressing to severe COVID-19 and 70% for all patients
  • Patients who were treated with regdanvimab (CT-P59) reported a significantly shortened time to clinical recovery by at least 4.7 days quicker for patients at high- risk of progressing to severe COVID-19 and by 4.9 days quicker compared to placebo for all patients
  • According to the recently published article from Biochemical and Biophysical Research Communications, sufficient antiviral effect in B.1.351 variant (now classified by the WHO as Beta)-infected animals was confirmed with a clinical dosage of regdanvimab (CT-P59)1

FDA Action Alert: Blueprint, Orphazyme and Eton

 The month of June continues to be busy for the U.S. Food and Drug Administration (FDA). There are three PDUFA dates on the calendar for this week. Here’s a look.

Blueprint Medicines’ Avapritinib for Advanced Systemic Mastocytosis

Blueprint Medicines has a target action date of June 16, 2021, for its supplemental New Drug Application (sNDA) for avapritinib for adults with advanced Systemic Mastocytosis (SM). SM is a rare hematologic disorder that results in an overproduction of mast cells and the accumulation of mast cells in the bone marrow and other organs. This can lead to a range of debilitating symptoms, organ dysfunction and failure. Almost all cases of SM are driven by the KIT D816V mutation, which activates mast cells abnormally. Avapritinib is marketed as Ayvakit for unresectable or metastatic gastrointestinal stromal tumor (GIST) patients with a mutation called PDGFRA exon 18.

The submission was built on data from the registrational PATHFINDER trial in advanced SM. The trial demonstrated an overall confirmed response rate of 75%. It also included data from the PIONEER Part 1 trial that highlighted the impact of Ayvakit on skin manifestations in non-advanced SM.

In the company’s first-quarter report on April 29, Jeff Albers, chief executive officer of Blueprint, said, “With a potential U.S. approval for Ayvakit in advanced systemic mastocytosis in the second quarter, we are looking forward to welcoming a new era of precision medicines care for people living with this debilitating disease.”

Orphazyme’s Arimoclomol for Nieman-Pick Disease Type C

Orphazyme A/S has a target action date of June 17 for its NDA for arimoclomol to treat Niemann-Pick Disease Type C. Originally there was a PDUFA date in March, but the FDA extended the review period under a standard extension to complete the NDA review. The NDA remains under Priority Review and does not impede eligibility for a Pediatric Rare Disease Priority Review Voucher. The drug had previously received the FDA’s Fast-Track and Breakthrough Therapy Designations for NPC as well as Orphan Drug and Rare Pediatric Disease Designations.

Niemann-Pick disease Type C is a rare, genetic, progressively debilitating, and often fatal neurovisceral disease. It is part of a family of lysosomal storage diseases and is caused by mutations that result in a defective NPC protein. This results in lipids normally cleared by the lysosome to accumulate in various organs, including the brain.

Arimoclomal amplifies the production of heat-shock proteins (HSPs). These proteins can rescue defective misfolded proteins, clear protein aggregates, and improve lysosome function. It is an oral drug that can cross the blood-brain barrier. It is also being developed for Gaucher disease, sIBM, and ALS.

Eton’s Ephedrine Ready-to-Use Injection

Eton Pharmaceuticals has a target action date of June 18 for its NDA for ephedrine Ready-to-Use (RTU) injection. Eton has publicly said very little about this NDA, which is the third of four NDAs with PDUFA dates from the company and/or its partners from May 27 through August 6. RTU ephedrine injection is typically used to treatment hypotension during anesthesia. The company generally focuses on developing and commercializing treatments for rare diseases. The other PDUFA dates are May 27 (dehydrated alcohol injection); May 29 (zonisamide oral suspension); and August 6 (topiramate oral solution). On May 28, the company received a Complete Response Letter from the FDA over its NDA for dehydrated alcohol injection for the treatment of methanol poisoning. The CRL reported that the agency had completed the review but determined it could not be approved in its current form.

https://www.biospace.com/article/fda-action-alert-blueprint-orphazyme-and-eton/