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Friday, October 28, 2022

Soros Tops The List Of Midterm Election Mega-Donors

 As Statista's Anna Fleck reports, to date, he has offered up a hefty $128.5M to the Democratic party. Other big spenders include Elizabeth & Richard Uihlein, the founders of a shipping and packaging company, who spent a combined $70.2M on the Republican party campaign, and hedge fund manager Kenneth Griffin, who spent $65.9M, also on the Republican side. While Soros has spent far and away the most of any individual - at least double the next in line - as Statista's chart shows, most of this year’s top 8 mega donors are Republicans. The following chart shows a roundup of the top mega donors in the U.S., based on FEC data researched by The Washington Post.

Infographic: Midterm Election Mega-Donors | Statista

You will find more infographics at Statista

A range of personalities appear on this top roundup, from hedge fund managers to tech entrepreneurs. At only 30 years old, Sam Bankman-Fried is the youngest to make it onto the list, after having made millions off of cryptocurrency investments. Meanwhile, according to NPR, more than $1.6 billion in funding on TV ads has come from so-called “dark money groups” vying to boost GOP Senate candidates’ chances.

The 2022 U.S. midterms look set to smash previous fundraising records for the election rounds, having already raised some $2.5 billion so far, according to data compiled by Open Secrets.

https://www.zerohedge.com/political/soros-tops-list-midterm-election-mega-donors

Intensive BP Lowering Harmful in Acute Ischemic Stroke

 A large randomized trial that was investigating intensive lowering of blood pressure in acute ischemic stroke patients who had undergone mechanical thrombectomy has been stopped early because of safety concerns.

"Intensive control of systolic blood pressure to lower than 120 mm Hg should be avoided to prevent compromising the functional recovery of patients who have received endovascular thrombectomy for acute ischemic stroke due to intracranial large-vessel occlusion," the investigators conclude.

Results from the ENCHANTED2/MT trial were presented by Craig Anderson, MD, professor of neurology and epidemiology, University of New South Wales, Sydney, Australia, on October 28 at the 14th World Stroke Congress (WSC), which is taking place in Singapore.

The study was simultaneously published online in The Lancet.

"What our results have pretty convincingly shown is that in acute stroke patients who have undergone mechanical thrombectomy, lowering blood pressure down to a systolic of 120 mm Hg for 3 days is too low for too long. We shouldn't go that far down," Anderson told theheart.org | Medscape Cardiology.

Anderson said the trial has provided an important message for clinical practice.

"This result is not what we expected, but it is a definitive result and gives us a lower safety margin for blood pressure in acute ischemic stroke patients. This, in itself, is a big step forward."

He noted that the optimum blood pressure for these patients is not known.

"We need to do further trials to determine optimum blood pressure in these acute patients, but perhaps we should be aiming more towards 140 mm Hg," he suggested.

"But this trial shows us that in patients who have had successful clot retrieval with endovascular treatment for acute ischemic stroke, careful blood pressure management is important to avoid levels becoming too low. We have to make sure we don't overshoot down to 120 mm Hg or below."

The chair of the WSC session at which the trial was presented, Jeyaraj Pandian, MD, head of neurology at Christian Medical College, Ludhiana, India, who is the current vice-president of the World Stroke Organization, said: "This is a very important result. It has major practical implications."

As background, Anderson explained that elevated blood pressure is very common in patients who have an acute ischemic stroke, and the higher the blood pressure, the higher the chances of having a worse outcome.

"Theoretically, if we can control the blood pressure, we may be able to improve outcomes," he said.

In 2019, the first ENCHANTED trial reported that controlling blood pressure by a moderate amount ― to around 140 mm Hg, which is lower than currently recommended in the guidelines ― was linked to a reduction in bleeding complications of thrombolysis and appeared safe, but it did not improve recovery, Anderson noted.

"This trial was done before mechanical thrombectomy became routinely adopted, and this procedure has now become the standard of care for large-vessel occlusion strokes, but we don't know what we should do about blood pressure in these patients," he added.

A smaller French trial has suggested lowering blood pressure to 130 mm Hg, rather than a more liberal 130 – 180 mm Hg, was safe after successful mechanical thrombectomy, but there was no effect on functional outcome.

"In stroke patients with a large-vessel occlusion, blood pressure is often elevated to very high levels. There are wide ranges of opinions on what to do about this ― whether it should be lowered, and by how much," Anderson said. "We conducted the current ENCHANTED2/MT trial to look at this issue."

The trial randomly assigned patients who had undergone successful mechanical clot retrieval and reperfusion but whose blood pressure was still elevated to two groups. In one group, blood pressure was aggressively lowered to <120 mm Hg within 1 hour of reperfusion, and blood pressure was kept at this level for 3 days. In the other group, a more liberal approach was used: blood pressure was kept at 140 – 180 mm Hg.

The primary endpoint was disability, as measured by the Modified Rankin Scale (mRS) score at 90 days.

The study was started in China with the intention of expanding recruitment internationally. The planned enrollment was more than 2000 patients.

However, in March of this year, after 821 patients had been enrolled, the data safety monitoring board (DSMB) recommended that recruitment into the trial be suspended because of a safety signal. All of the patients who had been recruited were from China.

These patients were followed to obtain the 3-month outcome results, after which the DSMB recommended that the trial be stopped because safety was still a problem.

Mean systolic blood pressure was 125 mm Hg at 1 hour and 121 mm Hg at 24 hours in the more intensive-treatment group; it was 143 mm Hg at 1 hour and 139 mm Hg at 24 hours in the less intensive-treatment group, giving an adjusted mean difference over 24 hours of 18 mm Hg.

Worse Disability Scores

Results showed that the patients who underwent the more intensive blood pressure lowering had more disability at 3-month follow-up, with worse scores on a shift analysis of the mRS than those in the less intensive group (common odds ratio [OR], 1.37; 95% CI, 1.07 – 1.76).

The unfavorable shift in mRS scores in the more intensive group was consistent in adjusted sensitivity analysis, and there was no significant heterogeneity in the treatment effect on the primary outcome across all prespecified subgroups.

The incidence of death or neurologic deterioration at 7 days was higher in the more intensive-treatment group than the less intensive-treatment group (common OR, 1.53), and a between-group difference emerged at 24 hours.

The incidence of death or disability (mRS scores, 3–6) at 90 days was higher among patients in the more intensive-treatment group than the less intensive-treatment group (53% vs 39%; OR, 1.85; P = .0001).

Among those who survived, more patients in the more intensive-treatment group had major disability (mRS scores, 3–5) at 90 days than did patients in the less intensive-treatment group (43% vs 28%; OR, 2.07; = .0001).

No Difference in ICH or Severe Hypotension Episodes

The incidence of symptomatic intracranial hemorrhage, mortality, and serious adverse events did not significantly differ between the two groups. There were no significant differences in recurrent ischemic stroke events at 90 days, and no episodes of severe hypotension were reported as a serious adverse event.

"Our results show that intensive lowering of blood pressure appears to be associated with worsening physical disability. While there was no difference in mortality rates between the two groups, the lower blood pressure appeared to compromise the ability to recover from the stroke," Anderson said.

On the possible mechanism of harm, he suggested that the intensive blood pressure reduction might be interfering with blood flow through the injured part of the brain and impeding the ability to recover from the clot removal procedure.

What Levels Should be Aimed For?

Anderson stressed that it was important to have conducted this trial.

"Current guidelines recommend very conservative level of blood pressure in acute ischemic stroke patients ― to below 180 mm Hg. But no lower limit is recommended.

"Most clinicians aim for about the 140 mm Hg mark, but there is a large variation in opinion on what to do," he said. "Some doctors treat aggressively, believing that lower pressures could be beneficial in preventing bleeding and swelling, and others prefer to keep levels higher. Our results have helped to give some guidance on this."

Asked what he thought an optimum target would be, Anderson replied: "For now, I think a target of around 140 mm Hg systolic would be reasonable, and there is no evidence to move below that."

Yvo Roos, MD, professor of acute neurology at University Medical Center, Amsterdam, the Netherlands, a co-author of the ENCHANTED2/MT trial, also commented for theheart.org | Medscape Cardiology.

"The real importance of these study results is that they show that lowering blood pressure too much is detrimental on outcome. My personal interpretation, looking at the results of this study but also on the previous studies, is that we should aim for a target of 140–150 mm Hg. This is true for patients with recanalization therapy. For patients without any therapy, I would even be more careful in lowering blood pressure and recommend just staying below 180 mm Hg."

As to whether these results are generalizable to other populations, given that the patients were Chinese, Anderson noted that Asian people have higher rates of intracranial atherosclerosis and more blood pressure complications in the heart and kidney than White patients. Stroke management patterns also differ.

"These points raise questions about generalizability, and while I think this is an issue for consideration, I do not think it should detract from the clarity of these results," he commented.

The study is supported by grants from the Shanghai Hospital Development Center, the National Health and Medical Research Council of Australia, the China Stroke Prevention Project, Shanghai Changhai Hospital, the Science and Technology Commission of Shanghai Municipality, Takeda China, Genesis Medtech, and Penumbra. Anderson has received grants from the National Health and Medical Research Council and Medical Research Futures Fund of Australia, the UK Medical Research Council, Penumbra, and Takeda China.

World Stroke Conference: Presented October 28, 2022.

Lancet. Published online October 28, 2022. Abstract

https://www.medscape.com/viewarticle/983176

Online Gender-Affirming Services 'Can Be Appealing,' Often Don't Take Insurance

[Emphasis ours.]

 Some telemedicine companies offering gender-affirming hormone treatment offered an affordable alternative to traditional care models, a researcher reported at the Sexual Medicine Society of North America (SMSNA) annual meeting.

A review of available services from six direct-to-consumer platforms -- Folx Health, True U Clinic, QueerDoc, Q, TransClinique, and Plume -- found that all met World Professional Association for Transgender Health (WPATH) standards of informed consent for gender-affirming hormone therapy, and standards for regular laboratory work for treatment monitoring.

All offered hormone therapy and legal assistance with name changes. Some offered other gender care services, like puberty blockers, medical letters of support for surgery, and surgery referrals, according to Erin Jesse, MD, a urology resident at the University Hospitals Cleveland Medical Center.

Notably, these telemedicine platforms may increase access to cost-effective and culturally competent care for uninsured transgender and gender-diverse people: First-year costs for hormone therapy without insurance ($1,022-$1,428 for oral estradiol and $1,184-$1,668 for intramuscular testosterone therapy) were similar to what they would be at a tertiary center used for comparison ($1,184 for estradiol and $1,216 for testosterone).

Most of the direct-to-consumer platforms do not accept private insurance or Medicaid, which would be cost-prohibitive for many prospective patients, while the comparison tertiary center did accept insurance. But, Jesse noted, the convenience of the online-only platforms might make it worth it for many patients.

"There can be a lot of distress that comes from even just going into a doctor's office -- maybe it's your first time, you're not sure if that physician is familiar with transgender care, maybe you're not sure what other patients in the office are going to think," Jesse told MedPage Today.

Getting healthcare from home, virtually, is a "huge benefit" for the patients who are uncomfortable or feel a lot of discrimination in an office setting, Jesse said. She added that online platforms could be more appealing to rural patients and younger or more tech-inclined people.

For the analysis, Jesse and her fellow researchers queried Google to find U.S. gender-affirming care platforms in March of 2022. Payment models on the online platforms included pay-per-service or monthly membership, and researchers estimated costs for the tertiary center using an online cost estimator.

The study did not evaluate platforms based on WPATH guidelines beyond informed consent and lab work because these qualities were not readily assessed from looking at the websites.

Jesse noted that none of the six services offered mental or behavioral health services.

Part of this separation, along with the informed-consent model, could be to reduce the stigma associated with gender diversity, or the assumption that it goes hand-in-hand with mental illness. In some modalities of care, transgender patients are required to undergo a mental health evaluation to access gender-affirming care.

Though there's a high rate of gender dysphoria and mental health comorbidity, Jesse said, "If you don't have mental health comorbidities that are a problem, or interfering in your life, then having to jump through hoops and going and getting a mental health evaluation is just extra stigma, it's extra steps. It's almost demeaning to the patient."

"For these specific platforms, [gender dysphoria] is what these doctors treat, and so that's what they're good at, and that's what they're comfortable treating," said Jesse. "They draw a line in the sand basically."


Disclosures

Jesse and co-investigators reported no disclosures.

NIH Long COVID Initiative To Assess Pfizer's Antiviral Pill As Potential Treatment

 

  • The National Institutes of Health's $1 billion RECOVER Initiative has decided to study Pfizer Inc's  antiviral drug Paxlovid as a potential treatment for long COVID.
  • Long COVID involves more than 200 symptoms ranging from exhaustion and cognitive impairment to pain, fever, and heart palpitations that can last for months and even years following a COVID-19 infection.
  • Estimates of long COVID prevalence range from 5 to 50% of people who have had a COVID-19 infection. It affects people with mild and severe COVID-19, including children.
  • According to details posted on Clinicaltrials.gov, the randomized, placebo-controlled trial will test Pfizer's treatment or placebo in 1,700 adult volunteers.
  • The Duke Clinical Research Institute is supervising the study, scheduled to start on January 1, 2023.
  • Reuters reported that several patients reported improvements in their symptoms after taking Pfizer's antiviral treatment.
  • Paxlovid is currently authorized for use in the first days of a COVID infection to prevent severe disease in high-risk patients.
  • Some researchers found that naltrexone has been used to treat pain, fatigue, and brain fog months after a coronavirus infection.
  • Naltrexone is a medication primarily used to manage alcohol or opioid use disorder.

FDA: 'Not enough evidence' that Y-mAbs therapy improves overall survival

  Y-mAbs Therapeutics, Inc. (the “Company” or “Y-mAbs”) (Nasdaq: YMAB) a commercial-stage biopharmaceutical company focused on the development and commercialization of novel, antibody-based therapeutic products for the treatment of cancer, today announced the outcome of the meeting of the U.S. Food and Drug Administration (“FDA”) Oncologic Drugs Advisory Committee (“ODAC”), which reviewed investigational 131I-omburtamab (“omburtamab”) for the treatment of CNS/leptomeningeal metastasis from neuroblastoma. The committee voted 16 to 0 that the Company had not provided sufficient evidence to conclude that omburtamab improves overall survival.

“We are disappointed by the outcome of today’s meeting, as patients with CNS/leptomeningeal metastasis from neuroblastoma are in need of effective and safe treatment options,” said Thomas Gad, President, and Interim Chief Executive Officer. “Y-mAbs is committed to working closely with the FDA on their review of the Biologic License Application (“BLA”) for omburtamab ahead of their decision. We want to thank all of the patients, caregivers, and healthcare providers who participated in the studies of this life-threatening condition.”

ODAC reviewed data from omburtamab’s clinical development program with a focus on study 03-133 (a pivotal phase 1 study) and study 101 (a pivotal phase 2 study) as well as the historical control group.

Y-mAbs BLA submission for omburtamab was accepted for Priority Review by the FDA on May 31, 2022, with a Prescription Drug User Fee Act (“PDUFA”) target date of November 30, 2022. The FDA is not bound by the Advisory Committee’s recommendations but generally takes the recommendation into consideration when making its decision.

Researchers at MSK developed omburtamab, which is exclusively licensed by MSK to Y-mAbs. As a result of this licensing arrangement, MSK has institutional financial interests in the compound.

https://finance.yahoo.com/news/y-mabs-announces-outcome-fda-193300494.html

Amicus: FDA Defers Action on Filing for AT-GAA in Late-onset Pompe Disease

 FDA Issues Deferred Action Letter on AT-GAA Regulatory Filing Due to the Inability to Conduct Required Manufacturing Site Inspection Prior to the PDUFA Action Date

Company is Now Actively Engaged with the Agency to Develop Plans and Logistics for a Pre-Approval Inspection

Amicus Therapeutics (Nasdaq: FOLD) today announced that the U.S. Food and Drug Administration (FDA) has deferred action on the Biologics License Application (BLA) for cipaglucosidase alfa, the biologic component of AT-GAA. Due to restrictions on travel related to COVID-19, the FDA was unable to conduct the required inspection of the WuXi Biologics manufacturing site in China during the review cycle. As a result, the FDA is deferring action on the application until the manufacturing site inspection is complete. The Company continues to expect the FDA to approve the two components of AT-GAA, including the BLA and New Drug Application (NDA) for miglustat, together.

The sole reason cited in the FDA-issued letter for the deferred action was the Agency’s inability to complete the manufacturing facility inspection. While both applications remain under review, the FDA has not provided anticipated action date(s) as they continue to monitor the public health situation and travel restrictions in China. However, the Company is now actively engaged with the FDA on developing plans and logistics for a pre-approval inspection plan.

Under FDA guidance relating to pre-approval inspections during the COVID-19 pandemic, the Agency may defer action on a pending application when a facility inspection is necessary but cannot be completed by the PDUFA goal date due to travel restrictions, provided that no deficiencies have been identified and the application otherwise satisfies the requirements for approval.



https://finance.yahoo.com/news/u-fda-defers-action-filing-200100759.html