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Thursday, September 1, 2022

Anti-Aging Supplement Might Actually Work

 My wife recently texted me about a new study out of the Baylor College of Medicine on a combination supplement, “GlyNAC,” with strongly positive data about its use in elderly patients. It claimed an outright plethora of age reversing benefits. I assumed the study would be an embarrassment of flaws. However, when I actually read it, I was surprised: this actually seems promising! Why had I not heard of it?

I had to dig around to find any reporting on it at all, outside of Baylor, which clearly needs to bolster their PR department. Well, at least the Bluff City area heard about this study, even if the bulletin got the medical college wrong:

The short-ish story on the trial, which was published in the peer-reviewed Journals of Gerontology, Series A, is that it was small (11 overweight adults, average age 71, in the GlyNAC group, and 12 in the placebo group), looked at a bushel of lab and clinical endpoints, and came out of the group, headed by Dr. Rajagopal V Sekhar, MD, which had published almost all the existing research on this combination of glycine and N-acetyl cysteine. Not encouraging, I know. But at least there were no conflicts of interest, right?

Good. Well, actually… not so good. The Baylor press release ‘fessed up to this little gem:

So, we have research conducted at an institution with a vested interest in its success, all sitting in the back pocket of one of the most reviled mega-corporations in the universe! Not an ideal combination. The data, though, is rather bewitching.

It’s a double-blinded, randomized, placebo-controlled trial, for starters, unlike the group’s prior (also encouraging but even smaller) study, which was open label, meaning researchers and participants knew what they were taking. Despite a scattershot endpoint approach which puts my inner skeptic on highest alert — including 5 measures of physical function, 5 of body composition, 25 “Hallmarks of Aging” laboratory biomarkers, a slate of metabolic labs, systolic and diastolic blood pressure, and a Quality of Life survey — the results are hard to dismiss. As I discussed in my tepid review of another mitochondrial-targeted supplement, Urolithin A, if you pick enough endpoints, a few are likely to pop up positively enough, even if only by chance, to generate some headlines and selling points for your product. In the case of GlyNAC, though, almost all their endpoints were positive.

Weight loss? Almost 5 pounds in 4 months. Blood pressure? From a mean of 132/79 to 124/76. Blood sugar barely budged, but insulin levels dropped a remarkable — practically unbelievable — two-thirds. Gait speed and chair-rise testing improved almost to the level of the young adult (25 year old average) comparator group. Grip strength improved to beyond the young adult levels! This was no placebo effect - there was virtually no improvement in any category for the placebo participants. As to the lab tests, nearly every single one of the biochemical markers for aging, inflammation, mitochondrial function, etc. showed a statistically significant improvement, often many times that of the placebo.

So, the next question has to be: does this make any sense? There is some biological plausibility here. NAC, as any ER doctor will tell you, plays an extremely effective role with both IV and oral forms in preventing liver failure after Tylenol overdoses. The mechanism of action is thought to be via supporting the activity of the critically-important intracellular and mitochondrial antioxidant, glutathione. Glycine is also known as a glutathione precursor, and has been found to have all sorts of possible benefits, from its function as a calming neurotransmitter to improving metabolic health.

The authors assert that by combining glycine and NAC, and thereby also increasing available glutathione, all three compounds work independently and together in a manner they term, the “power of three.” Yes, they actually wrote, “power of three,” with italics, in a peer-reviewed scientific journal. It almost sounds like… a marketing theme is born?

That really sums up this supplement for me. It sounds great, it looks great, but it smells a little fishy.

Maybe the authors have hit on two straight — really three, since they also published a 2013 study with mouse and human participants featuring similarly positive results — remarkably lucky trials that benefited from the potential random effects of a tiny sample size. Or maybe there is something rotten in the state of Denmark.

I have absolutely no reason to suspect Dr. Sekhar of foul play, but hypotheticals of misreported data, coached participants, or outright fabrication have to be considered whenever a study reports results that seem almost too good to be true. Ivermectin’s “100% effective” prophylaxis in an Argentina study that probably never happened comes to mind; as does that 2012 study on how to promote honesty which was — you guessed it — fabricated; and, recently, the disturbing allegations that seminal work on a branch of the amyloid hypothesis of Alzheimer’s disease was fraudulent. This stuff happens in science. There’s a lot of pressure to create winning research.

All that said, I am inclined to take this work at face value. I hope some of my patients will volunteer themselves as guinea pigs, though keeping in mind that this trial did not find benefit for young healthy folks, and the study group was composed of overweight seniors in relatively good health; results might not apply to a lean and chipper 70-year-old, or an 80-year-old diabetic with advanced kidney disease. I do like the ease of testing facilitated by the study design: run baseline labs including fasting glucose and insulin, perhaps a cholesterol panel and an inflammatory marker like high-sensitivity CRP; perform a cognitive test like the Montreal Cognitive Assessment (“MoCA”), since the prior study showed a marked improvement in MoCA scores; have patients perform a 30 second chair stand test; and ask them to see how far they can walk at a rapid pace in 6 minutes at the local track. Take the GlyNAC for 3-4 months. Rinse, lather, and repeat testing.

For those inclined to do the same (after consultation with their doctors, of course), I will point out that our dear friends at Nestlé sell their proprietary GlyNAC product as “Celltrient Cellular Protect.” However, the doses used in the trials were rather huge: 100 mg per kg per day, or about 7000mg each of NAC and glycine for an average weight adult. For reference, this is about double the maximum of what I ever recommend for NAC (I sometimes suggest it for hard-to-treat lung ailments given some encouraging data), and about twice the typical “full” glycine dose. The Celltrient product only contains 1200mg of each, and sells on their website for about $70 per 28 day supply. A 185-pound person would need about 7 of those packets every day at around $500 a month to match the study protocol!

While I won’t name any names, the more reputable supplement brands charge about $5/day for that amount of NAC, while the less expensive brands are about a third the price. Glycine is relatively cheap; it can be bought by the kilogram for $25. I do worry about quality controls from really inexpensive supplement makers, especially when consuming massive amounts of their products.

I might be talking myself out of trialing this cocktail with my patients. That’s a roughly $1000 experiment to run for four months, plus two sets of labs. (And, yes, the benefit appeared to evaporate once the supplement was stopped.) Lower doses might fare as well, I suppose, but another trial run by different investigators — many of them on Nestlé’s payroll — found only marginal benefit in biomarkers with higher dose ranges, and none in the 1200mg cysteine/1200mg NAC dosing found in the Celltrient product.

That leaves the wealthy and/or desperate to give this regimen a try. I’ll update this post if I get any takers. In a perfect world, the NIH will find and support a different research team to attempt to replicate these findings. Long term safety of these huge doses would need to be tracked; a reader pointed out to me that NAC mega-dosing is not without health concerns. To be clear, though, if these findings were replicated, it would be a huge deal. Reversing cognitive, physical, and metabolic age-related decline with a well-tolerated supplement would fall in the “Discovery of the Decade” category. It would be a complicated mess, financially, but someone other than Nestlé would need to patent a formulation of this and produce it, and insurance would have to pay for it.

In our imperfect world? Nestlé with its growing supplement empire will continue to be the sole force behind research on GlyNAC, and we physicians will never be sufficiently convinced to recommend it; and those lacking the resources to trial incredibly expensive supplements will never know if GlyNAC was “the one that got away.”

Buzz Hollander MD

Family Physician on the Big Island of Hawaii. 

US FDA approval tracker: August 2022

 It was a double FDA thumbs-up for Astrazeneca and Daiichi Sankyo’s Enhertu last month as the antibody-drug combo became the first Her2-targeted agent approved in Her2-positive lung cancer and Her2-low breast cancer. Enhertu looks set to dominate the Her2-low space, a newly defined subset in breast cancer, as competitors are still some way behind. Bluebird also received approval for Zynteglo, a gene therapy for transfusion-dependent beta-thalassaemia, but the company has a huge commercial task ahead to try and make the product profitable. Bluebird’s second gene therapy, eli-cel, has a Pdufa date in September, this time for cerebral adrenoleukodystrophy, a rare metabolic disorder. Investors will have to wait a little longer for several pending FDA decisions, including J&J’s multiple myeloma bispecific Tecvayli, which gained European approval in fourth-line disease last month. 

Notable first-time US approval decisions in August
ProjectCompanyIndication(s)2028e sales by indication (SBI) ($m)Outcome
Auvelity
(AXS-05)
AxsomeMajor depressive disorder787Approved
Neutrolin/
Defencath
CormedixPrevention of catheter-related bloodstream infections 392CRL (second, this time due to deficiencies at CMO)
XenpozymeSanofiNon-CNS manifestations of acid sphingomyelinase deficiency (Niemann-Pick disease) in adult and paediatric patients346Approved (~1 month early)
Miglustat for AT-GAAAmicusPompe disease266*No decision yet (part of two-component therapy with cipaglucosidase, Pdufa in Oct)
Tecvayli (teclistamab)Johnson & JohnsonR/R multiple myeloma 260No decision yet
Betibeglogene autotemcel (Zynteglo/ beti-cel)BluebirdBeta-thalassaemia (pts requiring regular red blood cell transfusions)120Approved
Libervant (diazepam) buccal filmAquestiveAcute treatment of intermittent, stereotypic episodes of frequent seizure activity90Tentative approval (Neurelis' Valtoco has orphan drug exclusivity)
Annik (penpulimab)Akeso/Sino3L nasopharyngeal carcinoma-No decision yet
*Forecast for AT-GAA. Source: company releases & Evaluate Pharma.
 
 
Private companies with pending FDA approvals
ProjectCompanyIndicationOutcome
SH-111Shorla OncologyUndisclosed project for T-cell leukaemiaPending (was filed in Apr 2021)
SpesolimabBoehringer IngelheimGeneralised pustular psoriasisDecision expected by YE
Source: company releases & Evaluate Pharma.

 

Supplementary and other notable approval decisions in August
ProductCompanyIndication (clinical trial)Outcome
NuplazidAcadiaHallucinations and delusions associated with Alzheimer's disease psychosis (Harmonyphase 2)CRL (new study required)
MyfembreePfizer/
Myovant
Moderate to severe pain associated with endometriosis (Spirit 1Spirit 2)Approved
EnhertuAstra/Daiichi Sankyo2L Her2-positive NSCLC (Destiny-Lung01Destiny-Lung02)Approved (accelerated)
Unresectable metastatic Her2 low breast cancer (Destiny-Breast04)Approved (~2 months early)
Cimerli (CHS-201/ FYB201, Lucentis biosimilar)Teva/Bioeq/
Formycon/
Coherus
Wet AMD, macular oedema following retinal vein occlusion, DME, diabetic retinopathy, and myopic choroidal neovascularisationApproved
Haloette (generic Nuvaring)Mayne Pharma/
Mithra
Vaginal hormonal contraceptive ringApproved (three previous CRLs)
Nubeqa + docetaxelBayer/
Orion
Metastatic hormone-sensitive prostate cancer (Arasens)Approved
Calquence tabletAstrazenecaAdult patients with chronic lymphocytic leukaemia, small lymphocytic lymphoma and for patients with relapsed or refractory mantle cell lymphoma (Elevate-Plus)Approved
XofluzaRocheTreatment of influenza in children aged 5-12, and for the prevention of influenza following contact with someone with influenza (oral therapy) (Ministone-2Blockstone)Approved
Hadlima (High concentration Humira biosimilar) (SB5)Samsung Bioepis/OrganonRA, juvenile idiopathic arthritis, psoriatic arthritis, ankylosing spondylitis, Crohn's, ulcerative colitis, plaque psoriasis (NCT04514796)Approved (launch expected on/after July 1 2023)
TabrectaNovartisAdult patients with metastatic NSCLC whose tumours have a mutation leading to MET exon 14 skipping (Geometry mono-1)Full approval (accelerated approval granted 2020)
PemazyreIncyteMyeloid/lymphoid neoplasms with FGFR1 rearrangement (Ph2 Fight-203)Approved
ImbruvicaJ&JPaediatric patients one year and older with chronic graft-versus-host disease after failure of one or more lines of systemic therapy (Ph1/2 Imagine)Approved
Source: company releases & Evaluate Pharma.

 

FDA EUAs
ProductCompanyIndication/outcome
JynneosBavarian NordicApproved for use in individuals determined to be at high risk for monkeypox infection
NuvaxovidNovavaxPrevention in Covid-19 in individuals aged 12-17 years old (vaccine, first granted an EUA in July)
Bivalent Covid-19 vaccineModernaFor use as a booster dose, includes original Sars-Cov-2 strain and omicron variant
Bivalent Covid-19 vaccinePfizer/Biontech
Source: FDA, company releases & Evaluate Pharma.

https://www.evaluate.com/vantage/articles/insights/nme-approvals-snippets/us-fda-approval-tracker-august-2022

Nevro: Positive Coverage Updates for Treatment of Painful Diabetic Neuropathy

 Aetna Updates Spinal Cord Stimulation Coverage Policy to Include Painful Diabetic Neuropathy Effective Immediately

Medicare Administrative Carriers Novitas and First Coast Propose Positive Local Coverage Determinations

https://www.biospace.com/article/releases/nevro-announces-multiple-positive-coverage-updates-for-the-treatment-of-painful-diabetic-neuropathy/

Wuhan Lab Linked to COVID-19 Discovers Novel Animal Virus

 Researchers at the Wuhan Institute of Virology (WIV), which is possibly linked to the origins of COVID-19, reported the discovery of a novel DNA virus in animals in the journal Virologica Sinica

The scientists analyzed tissue specimens from 232 animals, including 226 rodents, five shrews and one hedgehog, collected from five counties in Kenya and tested for DNA viruses. The viruses belong to seven viral families, and the researchers utilized PCR to run the tests. They noted that although surveillance programs focus more on RNA viruses - such as SARS-COV-2, the virus that causes COVID-19 - less is known about DNA viruses. 

The researchers identified a range of DNA sequences associated with adenoviruses, adeno-associated viruses, herpesviruses and polyomaviruses. Conducting phylogenetic analyses, they found most were distinct from previously described viruses. They also noted this was the first report of a full-length genomic characterization of a polyomavirus in Lemniscomys species.

The virus was dubbed LsPyV KY187 and “has less than 60% amino acid sequence identity to the most related Glis glis polyomavirus 1 and Scirus carolinensis polyomavirus 1 in both large and small T-antigen proteins, and thus can be putatively allocated to a novel species within Betapolyomavirus,” the authors wrote. 

Viruses Not Known to be Transmissible to Humans

“The results of this study are important for our understanding of viruses and their evolution in non-human animals,” Sean Beckmann, Ph.D., assistant professor of biology at Stetson University in Florida, who was not involved in the study, told BioSpace. “However, these findings should be taken in context. None of the viruses identified, or the novel viruses, are known to be transmissible to humans, and the authors don’t make any claims about their pathogenicity.” 

The authors emphasized that the research supports the need to continue studying rodent-borne viruses in East Africa. In addition, because the new virus does not appear to be closely related to any known pathogens, its effect on humans is “unclear and needs to be further assessed,” the researchers stated. 

Beckmann was equally cautious. “These findings are still valuable and important, but they shouldn’t be a cause for alarm that a bunch of new human pathogens have been found. Among the viruses that were identified, we don’t have any evidence of rodent to human transmission within those groups," he said. 

WIV and its Link to COVID-19 Transmission Theories 

The WIV is a leading research institute that focuses on viruses, but its possible association with the origins of COVID-19 has increased scrutiny of its operations.

There are two primary theories about the origin of COVID-19: the “lab-leak” theory and the “wet market” theory. The lab-leak theory argues the virus likely originated in bats, which were studied at the WIV, and then was accidentally released from the laboratory, possibly by an infected staffer. The wet market theory proposes that the virus originated in bats, moved to an intermediary animal at the Huanan Seafood Wholesale Market in Wuhan, and then to humans. The market is a few miles from the WIV. 

In addition to researchers at WIV, the Kenya study was conducted by investigators from the Chinese Academy of Sciences in Wuhan, China, the Mammalogy Section of the National Museums of Kenya, the Veterinary Services Department of the Kenya Wildlife Service and the Institute of Biotechnology Research, Jomo Kenyatta University of Science and Technology in Nairobi, Kenya.

The authors noted, “Emergence and re-emergence of infectious diseases of wildlife origin have led pre-emptive pathogen surveillances in animals to be a public health priority.” 

Beckmann concurred, telling BioSpace, “Since the emergence of COVID-19 (SARS-CoV-2), there has been increased attention and focus on the potential for other virus/bacteria/etc. to spill over from non-human animals to humans. This is long overdue, and these results do demonstrate the type of information we can gain."

https://www.biospace.com/article/wuhan-lab-potentially-linked-to-covid-19-discovers-novel-animal-virus-/

Shuttle Pharmaceuticals Commences Trading on Nasdaq Under Ticker Symbol "SHPH"

 Shuttle Pharmaceuticals Holdings, Inc. (Nasdaq: SHPH), a discovery and development stage specialty pharmaceutical company focused on improving the outcomes of cancer patients treated with radiation therapy (RT) while reducing its side effects, is pleased to announce the Company's shares of common stock has commenced trading on The Nasdaq Capital Market under the ticker symbol "SHPH".


Historically, the major advances in radiation oncology have focused on improving technology to increase the amount of radiation that can be administered to a tumor without damaging adjacent, normal tissues. Examples of other such technologies include intensity modulated radiation therapy (IMRT), stereotactic body radiation therapy (SBRT), stereotactic radiosurgery (SRS) and proton therapy – the backbones of state-of-the-art RT. All offer improvements in physical radiation dose shaping. The basic principle underlying the effectiveness of RT for curing cancers lies in the differential cancer cell kill achieved in tumors, as compared to the effects of RT on the normal surrounding tissues, which is achieved by delivery of highly conformal RT doses – in other words, delivery of high-dose to volumes that are shaped to conform to the target cancers while minimizing the dose to surrounding normal tissues. The treated volumes frequently include sensitive normal tissues, thereby limiting the magnitudes of the prescribed RT doses. We suggest that technological innovations to define tumor volumes and shape radiation delivery have reached an effectiveness plateau and that further improvements in RT outcomes will require pharmacological and immunological approaches to sensitize cancers, protect normal tissues and engage the immune system.

https://finance.yahoo.com/news/shuttle-pharmaceuticals-commences-trading-nasdaq-172000516.html

Celsion: Progress in DNA-based Vaccine Program with covid virus

 Celsion Corporation (NASDAQ: CLSN), a clinical-stage company focused on DNA-based immunotherapy and next-generation vaccines, today provided an update on the progress made in the development of a DNA-based vaccine using its PLACCINE platform technology. Additional data from its completed proof-of-concept mouse challenge study confirms that a PLACCINE vaccine can produce robust levels of IgG, neutralizing antibodies, and T-cell responses.

The Company previously reported evidence of IgG, neutralizing antibody, and T-cell responses to its SARS-CoV-2 PLACCINE vaccines in normal mice. The additional data from its now completed mouse challenge study demonstrates the ability of the Company’s PLACCINE vaccine to protect a SARS-CoV-2 mouse model in a live viral challenge. In the study, mice were vaccinated with a PLACCINE vaccine expressing the SARS-CoV-2 spike antigen from the D614G variant or the Delta variant, or a combination vaccine expressing both the D614G and Delta spike variants. The vaccination was administered by intramuscular injection on Day 0 and Day 14, followed by challenge with live SARS-CoV-2 virus on Day 42. All three vaccines, including the single and dual antigen vaccines, were found to be safe and elicited IgG responses and inhibited the viral load by 90-95%. The dual antigen vaccine was equally effective against both variants of the SARS CoV-2 virus.

https://finance.yahoo.com/news/celsion-corporation-highlights-progress-dna-123000113.html

Vaxart: Positive Top-line Phase II Data for COVID-19 Pill Vaccine

 Study met primary safety and secondary immunogenicity endpoints 

 Boosted serum neutralizing antibodies in both naive and previously mRNA vaccinated subjects 

 Elicited cross-reactive mucosal responses in approximately 50% of subjects 

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

The Vaxart senior management team will host a conference call today, beginning at 8:30 a.m. ET.

The conference call can be accessed using the following information:
Webcast: Click here
Date: Thursday, September 1, 2022 – 8:30 a.m. ET
Domestic: 877-407-0832
International: 201-689-8433
Conference ID: 13732510

Investors may submit written questions in advance of the conference call to ir@vaxart.com. A replay of the webcast will be available on the Company’s website at www.vaxart.com following the conclusion of the event.

https://finance.yahoo.com/news/vaxart-announces-positive-top-line-103000580.html