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Monday, October 3, 2022

RedHill: Oral Broad-Acting Antivirals Inhibit Dominant Omicron Sub-Variant BA.5

 

  • RedHill Biopharma Ltd  announced study results showing in vitro efficacy against the currently dominant omicron COVID-19 sub-variant BA.5, by both RedHill's broad-acting investigational antivirals once-daily RHB-107 (upamostat) and twice-daily opaganib.
  • These results build on previously reported data on the inhibition of COVID-19, variants of concern, and other viruses and further support their broad-acting, host-directed mechanisms of action.
  • RHB-107 recently reported positive results from the Phase 2 part of Phase 2/3 study in symptomatic non-hospitalized COVID-19, showing good safety and tolerability and highly promising efficacy results, including faster recovery from severe COVID-19 symptoms and reduced rates of hospitalization.
  • Opaganib has previously demonstrated a 70% reduction in mortality in key hospitalized patient sub-populations, improved viral RNA clearance, and faster time to recovery in its Phase 3 study in hospitalized patients with moderate to severe COVID-19.
  • Late-stage development of both opaganib and RHB-107 is ongoing pending Phase 3 trial design regulatory approvals and securing of external funding.

Severe Sleep Apnea Diagnosis Panics Reporter Until He Finds a Simple, No-Cost Solution

I woke up in a strange bedroom with 24 electrodes glued all over my body and a plastic mask attached to a hose covering my face.

The lab technician who watched me all night via video feed told me that I had "wicked sleep apnea" and that it was "central sleep apnea" — a type that originates in the brain and fails to tell the muscles to inhale.

As a journalist — and one terrified by the diagnosis — I set out to do my own research. After a few weeks of sleuthing and interviewing experts, I reached two important conclusions.

First, I had moderate apnea, if that, and it could be treated without the elaborate machines, mouthpieces, or other devices that specialists who had consulted on my care were talking about.

Second, the American health care system has joined with commercial partners to define a medical condition — in this case, sleep apnea — in a way that allows both parties to generate revenue from a multitude of pricey diagnostic studies, equipment sales, and questionable treatments. I was on a conveyor belt.

It all began with a desire for answers: I had been feeling drowsy during the day, and my wife told me I snored. Both can mean obstructive sleep apnea. With obstructive sleep apnea, the mouth and throat relax when a person is unconscious, sometimes blocking or narrowing the airway. That interrupts breathing, as well as sleep. Without treatment, the resulting disruption in oxygen flow might increase the risk of developing certain cardiovascular diseases.

So I contacted a sleep-treatment center, and doctors gave me an at-home test ($365). Two weeks later, they told me I had "high-moderate" sleep apnea and needed to acquire a continuous positive airway pressure, or CPAP, machine, at a cost of about $600.

Though I had hoped to get the equipment and adjust the settings to see what worked best, my doctors said I had to come to the sleep lab for an overnight test ($1,900) to have them "titrate" the optimal CPAP air pressure.

"How do you treat central sleep apnea?" I worriedly asked the technician after that first overnight stay. She said something about an ASV (adaptive servo-ventilation) machine ($4,000). And one pricey lab sleepover wasn't enough, she said. I needed to come back for another.

(Most procedures and devices mentioned in this article were covered or would have been covered by insurance — in my case, Medicare, plus a supplemental plan. Unnecessary care is a big reason Americans' insurance costs — premiums, copays, and deductibles — tend to rise year after year.)

As a journalist who spent years covering the business of health care, I found there was more motivating my expensive testing cascade than concerns about my health.

The American Academy of Sleep Medicine, or AASM, a nonprofit based near Chicago, decides what is sleep apnea and how to treat it. Working with sleep societies around the world, it publishes the International Classification of Sleep Disorders, relied on by doctors everywhere to diagnose and categorize disease.

But behind that effort lie considerable conflicts of interest. Like so much of U.S. health care, sleep medicine turns out to be a thriving industry. AASM finances its operations in part with payments from CPAP machine manufacturers and other companies that stand to profit from expensive treatments and expansive definitions of apnea and other sleep disorders.

Zoll Itamar, which makes the at-home testing device I used, as well as implantable nerve-stimulation hardware for central sleep apnea, is a $60,000, "platinum" partner in AASM's Industry Engagement Program. So is Avadel Pharmaceuticals, which is testing a drug to treat narcolepsy, characterized by intense daytime sleepiness.

Other sponsors include the maker of an anti-insomnia drug; another company with a narcolepsy drugFisher & Paykel Healthcare, which makes CPAP machines and masks; and Inspire Medical Systems, maker of a heavily advertised surgical implant, costing tens of thousands of dollars, to treat apnea.

Corporate sponsors for Sleep 2022, a convention AASM put on in Charlotte, North Carolina, with other professional societies, included many of those companies, plus Philips Respironics and ResMed, two of the biggest CPAP machine makers.

In a statement, AASM spokesperson Jennifer Gibson said a conflict-of-interest policy and a non-interference pledge from industry funders protect the integrity of the academy's work. Industry donations account for about $170,000 of AASM's annual revenue of about $15 million, she said. Other revenue comes from educational materials and membership and accreditation fees.

Here's what else I found. Almost everybody breathes irregularly sometime at night, especially during REM sleep, characterized by rapid eye movement and dreams. Blood oxygen levels also fluctuate slightly.

But recent European studies have shown that standards under the International Classification of Sleep Disorders would doom huge portions of the general population to a sleep apnea diagnosis — whether or not people had complaints of daytime tiredness or other sleep problems.

study in the Swiss city of Lausanne showed that 50% of local men and 23% of the women 40 or older were positive for sleep apnea under such criteria.

Such rates of disease are "extraordinarily high," "astronomical," and "implausible," Dr. Dirk Pevernagie, a scientist at Belgium's Ghent University Hospital, wrote with colleagues two years ago in a comprehensive study in the Journal of Sleep Research.

"Right now, there is no real evidence for the criteria that have been put forward to diagnose obstructive sleep apnea and rate its severity," he said in an interview.

Likewise, 19% of middle-aged subjects in a 2016 Icelandic study appeared to have moderate to severe "apnea" under one definition in the International Classification of Sleep Disorders even though many reported no drowsiness.

"Most of them were really surprised," said Erna Sif Arnardóttir, who led the study and is running a large European program to refine detection and treatment of apnea.

Nevertheless, the official AASM journal recommends extremely broad screening for sleep apnea, looking for patients who have what it defines as illness. Everybody 18 and older should be screened every year for apnea if they have diabetes, obesity, untreated high blood pressure, or heart disease — even if they have never complained about sleep problems, the group says.

AASM "continually evaluates the definitions, criteria and recommendations used in the identification of sleep apnea and other sleep disorders," Gibson said in the statement. Meanwhile, routine screening by primary care doctors "is a simple way" of gauging whether a high-risk patient may have obstructive sleep apnea, the statement said.

The U.S. Preventive Services Task Force, an authoritative body that reviews the effectiveness of preventive care, takes a conservative view, more like that of the European researchers, concluding there is "insufficient" evidence to support widespread screening among patients with no symptoms. 

Many insurers refuse to pay for CPAP machines and other treatments prescribed for people at the outer edges of the AASM's apnea definition. But AASM is pressuring them to come around.

After all my reporting, I concluded that my apnea is real, though moderate. My alarming reading in the overnight lab — diagnosed quickly as central sleep apnea — was a byproduct of the testing machinery itself. That's a well-described phenomenon that occurs in 5% to 15% of patients.

And when I looked closely at the results of my at-home diagnostic test, I had an epiphany: My overall score was 26 breathing interruptions and blood-oxygen level declines, on average, per hour — enough to put me in the "high-moderate" category for apnea. But when I looked at the data sorted according to sleeping positions, I saw that I scored much better when I slept on my side: only 10 interruptions in an hour.

So I did a little experiment: I bought a $25 pulse oximeter with a smartphone app that records oxygen dips and breathing interruptions. When I slept on my side, there were hardly any.

Now I sleep on my side. I snore less. I wake up refreshed. I'm not daytime drowsy.

None of my specialists mentioned turning on to my side — known in medical parlance as "positional therapy" — though the intervention is recognized as effective by many researchers. Sleeping on one's back contributes to snoring and blockages, especially as people age and the muscles in the throat become looser.

"Positional patients … can sleep in the lateral position and sleep quite well," said Arie Oksenberg, a sleep researcher formerly at Loewenstein Hospital in Israel.

But it's not easy to find this in the official AASM treatment guidelines, which instead go right to the money-making options like CPAP machines, surgery, central apnea, and mouth appliances.

Dealing with apnea by shifting slightly in bed gets little more than a couple of paragraphs in AASM's guideline on "other" treatments and a little box on a long and complex decision chart.

A third or more of patients wear CPAPs only a few hours a night or stop using them. It turns out people don't like machines in their beds.

"Positional therapy is an effective treatment option for some patients," said the AASM's Gibson. But she said there are concerns about whether patients will sleep on their sides long term and whether trying to stay in one position might cause sleep interruptions itself.

It's true that side-sleeping doesn't help everybody. And it often takes practice. (Some people tape a tennis ball to their pajamas to keep them off their backs.) Even conservative sleep doctors say CPAP machines are the best solution for many patients.

But there is a largely overlooked alternative.

"Are we missing a simple treatment for most adult sleep apnea patients?" was the name of a 2013 paper that Oksenberg and a colleague wrote about positional therapy.

In my case, the answer was "yes."

Jay Hancock is a former KHN senior correspondent.

https://www.medscape.com/viewarticle/981785

Athletes With Mild HCM 'Can Likely Continue Competitive Sports'

 Athletes with mild hypertrophic cardiomyopathy (HCM) at low risk of sudden cardiac death (SCD) can safely continue to exercise at competitive levels, a retrospective study suggests.

During a mean follow-up of 4.5 years, athletes who continued to engage in high-intensity competitive sports after a mild HCM diagnosis were free of cardiac symptoms, and there were no deaths, incidents of sustained ventricular tachycardia or syncope, or changes in cardiac electrical, structural, or functional phenotypes.

"This study supports emerging evidence that HCM individuals with a low-risk profile and mild hypertrophy may engage in vigorous exercise and competitive sport," Sanjay Sharma, MD, of St. George's University of London, UK, told theheart.org | Medscape Cardiology. Current guidelines from the European Society of Cardiology and the American College of Cardiology support a more liberal approach to exercise for these individuals, he noted.

That said, he added, "It is important to emphasize that our cohort consisted of a group of adult competitive athletes who had probably been competing for several years before the diagnosis was made and therefore represented a self-selected, low-risk cohort. It is difficult to extrapolate this data to adolescent athletes, who appear to be more vulnerable to exercise-related SCD from HCM."

The study was published online today in the Journal of the American College of Cardiology.

Vigorous Exercise OK for Some

Sharma and colleagues analyzed data from 53 athletes with HCM who continued to participate in competitive sports. The mean age was 39 years, 98% were men, and 72% were White. About half (53%) competed as professionals, and were most commonly engaged in cycling, football, running, and rugby.

Participants underwent 6 to 12 monthly assessments that included electrocardiograms (ECGs), echocardiograms, cardiopulmonary exercise testing, Holter monitoring (≥ 24 hours), and cardiac magnetic resonance (CMR) imaging. A majority (64.2%) were evaluated because of an abnormal ECG, and one presented with an incidental abnormal echocardiogram.

About a quarter (24.5%) were symptomatic and 5 (9.4%) were identified on family screening. Eight (15%) had a family history of HCM, and six (11.3%) of SCD.

At the baseline evaluation, all athletes had a "low" European Society of Cardiology 5-year SCD risk score for HCM (1.9% ± 0.9%). None had syncope. Mean peak VO2 was 40.7 ± 6.8 mL/kg/min.

The mean left ventricular (LV) wall thickness was 14.6 ± 2.3 mm. All had normal LV systolic and diastolic function and no LV outflow tract obstruction at rest or on provocation testing. In addition, none had an LV apical aneurysm.

Twenty-two (41%) showed late gadolinium enhancement on baseline CMR.

A total of 19 participants underwent genotyping; 4 (21.1%) had a pathogenic/likely pathogenic sarcomeric variant. None took cardiovascular medication or had an implantable cardioverter defibrillator (ICD).

During a mean follow-up of 4.5 years, all participants continued to exercise at the same level as before their diagnosis; none underwent detraining. All stayed free of cardiac symptoms, and there were no deaths, sustained ventricular tachycardia episodes, or syncope.

Four demonstrated new, nonsustained ventricular tachycardia (NSVT) during follow-up, one of whom underwent ICD implantation because of an increased risk score and subsequently moderated exercise levels.

One participant had a >30-second atrial fibrillation (AF) episode, started on a beta-blocker and oral anticoagulation, and also moderated exercise levels.

The event rate was 2.1% per year for asymptomatic arrhythmias (NSVT and AF). No changes were observed in the cardiac electrical, structural, or functional phenotype during follow-up.

Sharma and colleagues state, "Our sample size is small; however, it is nearly double the size of a previously studied Italian athletic cohort, and one half were professional athletes. Furthermore, 17% of our cohort comprised Black athletes who are perceived to be at higher risk of SCD than White athletes."

Daniele Massera, MD, assistant professor in the HCM Program, Department of Medicine, Charney Division of Cardiology, NYU Langone Health, New York City, commented on the study for theheart.org | Medscape Cardiology. "Of note, these were athletes/patients at the very low end of phenotypic severity of HCM...It is also notable that diastolic function was normal in all of them, an uncommon finding in patients with HCM."

Like Sharma, he said the findings are in line with recent guidelines, and cautioned, "This small study applies only to a very small subset of patients who are being evaluated at specialized HCM programs: asymptomatic male individuals who have mild, low-risk HCM and are on no medicines.

"The findings cannot be generalized to the population of symptomatic individuals with (or without) outflow obstruction, more severe hypertrophy, and who have ICDs and/or take medication for symptoms, nor to younger patients or adolescents, who may be at higher risk for adverse outcomes," he concluded.

Individualized Approach Urged

Sharma was a coauthor of the recent JACC article challenging the traditional restrictive approach to exercise for athletes diagnosed with HCM and other inherited cardiovascular diseases. The article suggested that individualized recommendations, taking risks into consideration, can help guide those who want to exercise or participate in competitive sports.

Sharma also is a coauthor of a 6-month follow-up to the SAFE-HCM study, which compared the effects of a supervised 12-week high-intensity exercise program to usual care in low-risk individuals with HCM (mean age, 45.7). 

In the 6-month follow-up study, published as an abstract in the European Journal of Preventive Cardiology 2021 supplement, "exercising individuals had improved functional capacity and atherosclerotic risk profile and there were no differences in the composite safety outcomes (CV death; cardiac arrest; device therapy; exercise-induced syncope; sustained VT; NSVT or sustained atrial arrhythmias) between exercising individuals and usual care individuals," Sharma said.

The full study will soon be ready to submit for publication, he added.

No commercial funding or relevant conflicts of interest were disclosed.

J Am Coll Cardiol. Published online October 3, 2022. Letter

https://www.medscape.com/viewarticle/981782

Traditional Glaucoma Surgery Tops Minimally Invasive for Treatment Success

 Traditional glaucoma surgery more than doubled the likelihood of treatment success for elevated intraocular pressure (IOP) as compared with the more widely used minimally invasive glaucoma surgery (MIGS), but with more complications, according to data from a national registry.

More than half of patients who had traditional incisional glaucoma surgery (TIGS) met criteria for treatment success at 1 year, as compared with about a fourth of patients who had MIGS procedures. The between-group differences were similar at 2 and 3 years. Investigators defined success as an IOP ≤18 mm Hg plus a reduction of ≥20% from baseline, with no hypotony (IOP ≤5 mm Hg), reoperation for glaucoma, or loss of light perception.

Both types of procedures significantly reduced IOP from baseline, but TIGS led to substantially larger decreases. The notable downside of TIGS was a higher rate of complications, including severe complications, said Shan Lin, MD, of the Glaucoma Center of San Francisco, during the American Academy of Ophthalmology (AAO) meeting.

"We're not very surprised [by the results]," said Lin. "MIGS real-world success is probably less than what we see in the published literature, randomized clinical trials. "There are many reasons for that, but we don't have time to go into that. There is a significant lowering of intraocular pressure [with MIGS] and medication use stayed about the same."

During a discussion that followed his presentation, Lin acknowledged that most MIGS procedures included placement of trabecular meshwork bypass stents, which could have influenced the impact of the surgery. Additionally, many of the patients treated with MIGS had cataract surgery at the same time, and studies have shown that cataract surgery alone has an IOP-lowering effect.

A member of the audience also pointed out that stents have improved over time and many of the devices included in the analysis "are no longer in play," which could have influenced the results with MIGS.

"That's a really good point," said Lin. "We're probably going to have better results with the newer MIGS."

The analysis involved data from the AAO's Intelligent Research in Sight (IRIS) Registry, the nation's first comprehensive eye disease registry based on electronic health records contributed by 7,200 practicing ophthalmologists. The analysis included procedures performed from Jan. 1, 2014 through Dec. 31, 2018, allowing for 3 years of follow-up in all cases. Eligible patients were 18 or older and had a diagnosis of primary open-angle glaucoma (POAG).

In addition to the primary outcome, two alternate analyses were performed with different IOP criteria: ≤21 mm Hg and ≤14 mm Hg.

Data analysis included 60,031 eyes, comprising 16,890 in the TIGS group and 43,141 in the MIGS group. TIGS procedures consisted of 9,666 trabeculoplasties and 7,224 tube shunts. In the MIGS group, 29,938 procedures included a bypass stent.

The patients had a median age of 71-73, women accounted for about 60% of the total population, and two-thirds of patients were white. In the TIGS group, 17.4% of procedures included concurrent cataract surgery, whereas 98.8% of MIGS procedures included cataract surgery. A majority (54.5%) of eyes in the TIGS group had severe POAG, and 87% of the MIGS group had mild or moderate POAG.

The primary analysis showed that 54.6% of TIGS procedures met success criteria as compared with 26.2% of the MIGS group. Mean IOP decreased from 24 to 14 mm Hg (a 42% reduction) in the TIGS group versus 17 to 15 mm Hg (10%) with MIGS, both of which represented significant improvement from baseline (P<0.001). Medication use decreased significantly (P<0.001) in the TIGS group after surgery and remained unchanged in the MIGS group, which had lower baseline medication use.

The most common reason for not achieving treatment success was failure to reduce IOP by ≥20% from baseline in both the TIGS (69%) and MIGS (97%) groups. In about a third of TIGS cases, IOP did not decline to ≤18 mm Hg as compared with a fourth of the MIGS group. Hypotony rates were 12% with TIGS and 0.4% with MIGS, reoperation rates were 14% versus 3%, and loss of light perception occurred in 2% and 0.1%, respectively.

Two years after surgery, 50.8% of the TIGS group still met criteria for treatment success as compared with 25.5% of the MIGS group, and the 3-year success rates were 46.6% versus 24.9%. When IOP reduction ≥20% from baseline was excluded from the success criteria, rates of treatment success at 1 year were 75% with TIGS and 83% with MIGS.

Severe complications (such as endophthalmitis, retinal detachment, and suprachoroidal hemorrhage) occurred more often with TIGS but were infrequent in both groups.

Lin acknowledged several limitations of the analysis: the lack of visual field data, multiple variables with a substantial "unknown" component, the potential for miscoding in data entry, and possible underreporting of complications and adverse events.


Disclosures

Lin disclosed relationships with Aerie Pharmaceuticals, Bausch + Lomb, Eyenovia, and Iridex.

Skin swab test could potentially detect Parkinson’s disease

 A team of researchers in the U.K. have developed a potential test for Parkinson’s disease in which they analyze skin swabs. 

Previous research suggests the potential ability to detect differences in types of sebum, the oily waxy substances produced by the skin, in people with Parkinson’s disease (PD). The chemical makeup of sebum in Parkinson’s patients may contain different fats and metabolites that can be detected using mass spectrometry, a technique that scientists use to identify molecules. 

Scientists pursued this line of thinking from observing Joy Milne, who can distinguish PD in individuals from a distinct body odor before clinical symptoms occur, according to a press release. Milne has a heightened sense of smell and was able to detect a difference in sebum that collects on the upper back of patients. 

For this test, clinicians can collect a skin swab from the upper backs of patients and send in the sample for analysis. The study has been published in the Journal of the American Chemical Society

“The sebum is transferred to filter paper from sampling swab, and we then cut this to a triangle, add a drop of solvent, apply a voltage and this transfers compounds from the sebum into the mass spectrometer,” lead author Depanjan Sarkar at the University of Manchester said in a statement. “When we do this, we find more than 4000 unique compounds of which 500 are different between people with PD compared to the control participants.” 

The molecular weights of the compounds found in sebum of Parkinson’s patients were significantly different than skin samples taken from people without Parkinson’s. 

The authors say that further work is necessary to understand how this kind of test could be used for diagnosis and clinical purposes, but this proof-of-concept is a step in that direction.

“This test has the potential to massively improve the diagnosis and management of people with Parkinson’s disease,” said another study author, Monty Silverdale, who is a neurologist from the University of Manchester in the U.K., in the press release. 

https://thehill.com/changing-america/well-being/medical-advances/3672272-skin-swab-test-could-potentially-detect-parkinsons-disease/

Novo Nordisk: Once-weekly insulin icodec demonstrates superior reduction in HbA1c

 Novo Nordisk today announced headline results from the ONWARDS 5 phase 3a trial with once-weekly insulin icodec in people with type 2 diabetes.

The ONWARDS 5 trial was a 52-week, open-label efficacy and safety treat-to-target trial investigating once-weekly insulin versus once-daily basal insulin (insulin degludec or insulin glargine U100/U300) in 1,085 insulin-naïve people with type 2 diabetes in a clinical practice setting including fewer trial visits compared to the other ONWARDS phase 3a trials. Once-weekly insulin icodec was used in combination with a dosing guide app to guide titration.

The trial achieved its primary endpoint of demonstrating non-inferiority in reducing HbA1c at week 52 with insulin icodec compared with once-daily basal insulin analogues. From an overall baseline HbA1c of 8.9%, once-weekly insulin icodec achieved a superior reduction in estimated HbA1c of –1.68%-points compared with –1.31%-points for the once-daily basal insulins (estimated treatment difference: –0.38%-points).

https://finance.yahoo.com/news/once-weekly-insulin-icodec-demonstrates-120200785.html

Aura Bio Phase 2 Choroidal Melanoma Data Disappoints

 Aura Biosciences Inc. (NASDAQ: AURA), a clinical-stage biotechnology company developing a novel class of virus-like drug conjugate (VDC) therapies for multiple oncology indications, today announced that interim Phase 2 data evaluating the safety and efficacy of suprachoroidal (SC) administration using its first VDC product candidate, belzupacap sarotalocan (AU‑011), for the first-line treatment of patients with early-stage choroidal melanoma (indeterminate lesions and small choroidal melanoma (IL/CM)), were presented at the American Academy of Ophthalmology (AAO) 2022 Annual Meeting held September 30-October 3, 2022, in Chicago, IL.

"The Phase 2 interim safety and efficacy data that was presented at AAO is very encouraging for patients with primary choroidal melanoma, as the majority of patients are diagnosed with early-stage disease and have no vision-preserving treatment options. Interim data showed a statistically significant reduction in tumor growth rate and a robust tumor control response with a high rate of visual acuity preservation at the therapeutic regimen," said Dr. Ivana Kim, Director of the Ocular Melanoma Center, Massachusetts Eye and Ear. "Belzupacap sarotalocan offers a favorable safety profile supporting the potential to become the first vision-preserving treatment for early-stage choroidal melanoma, where patients have had to rely on radiotherapy for the last few decades."

"Preliminary analysis of the data from the Phase 2 trial using suprachoroidal administration supports tolerability up to three cycles of therapy and shows a dose-dependent anti-tumor response. The results provide further clinical evidence to support the potential use of belzupacap sarotalocan as a novel targeted therapy in patients with early-stage disease with this targeted route using suprachoroidal administration," said Dr. Cadmus Rich, Chief Medical Officer and Head of R&D of Aura Biosciences. "We believe that the data to date provides proof of concept for an additional intraocular route of administration and further supports belzupacap sarotalocan’s target product profile."

https://finance.yahoo.com/news/aura-biosciences-announces-interim-phase-110000174.html