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HMNC aims to make ketamine treatment first-in-class for patients

The company hopes to improve access to ketamine treatment by delivering its therapies in at-home settings.

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Photo by Towfiqu barbhuiya on Unsplash

Chief clinical development officer of HMNC Brain Health, Hans Eriksson, speaks to Psychedelic Health about how the company’s formula, ‘Ketabon’, will provide the therapeutic benefits of ketamine without the ‘trip.’

In June 2022, HMNC and Develco Pharma’s Phase 2 oral prolonged-release ketamine (Ketabon) Study dosed its first patient. The trial aims to understand if ketamine can help people living with treatment-resistant depression (TRD) who have not responded to a minimum of two standard antidepressants in their current major depressive episode. 

See also  HMNC: pioneering precision medicine for psychiatric care

Based on the data, HMNC believes the pharmacokinetic profile of its prolonged release Ketabon formulation could significantly improve tolerability and patient convenience by minimising dissociative effects compared with the currently applied intravenous and intranasal therapies.

Ketabon

HMNC’s proprietary formulation of ketamine is an oral formulation of ketamine that is taken up slowly by the body, with its concentration peaking at around six to eight hours.

The formulation, delivered in pill form, contains both enantiomers of ketamine – (S)-ketamine and (R)-ketamine – explains Eriksson.

“Since it’s taken orally, everything will essentially pass by the liver, so, quite a lot of the parent compound, ketamine – an active compound – is metabolised, as we get the relatively higher contribution of some of the downstream active metabolites,” said Eriksson. 

See also  Activating a stress circuit in the brain may improve ketamine treatment

“We believe that some of the advantages that we expect to find with Ketabon come from the pharmacokinetic properties, both the slow concentration buildup and also the relatively high first-pass metabolism.” 

In its Phase 1 study, results demonstrated that patients with chronic pain conditions that were exposed to this compound had good tolerability. 

A smaller Phase 2 study in treatment-resistant depression was conducted in an academic setting at the University of Zurich in Switzerland, although the study was terminated early due to difficulties in recruiting participants during the pandemic.

“This study still gave us lots of encouragement because we saw a clear signal of clinical efficacy,” said Eriksson. 

See also  Five-year study shows single ketamine dose reduces suicidal thoughts

With HMNC’s larger Phase 2 study underway, a clinical data readout is expected during the first half of next year. This study is being carried out with 117 patients in three different treatment arms as an add-on to standard antidepressant treatment in three countries in Europe. It is also being run as an outpatient study, which is not very usual for ketamine.

The first dose in the study is being given under medical supervision to ensure safety. While the study aims to demonstrate efficacy and safety, it is also an exploratory study, says Eriksson, as HMNC believes that three weeks may not be essential to achieve maximum efficacy. 

“We believe that sometime during the time after three weeks there will be maximum efficacy,” said Eriksson. “That’s probably the induction phase that we will use going forward as there is quite a lot of compelling evidence that maintenance treatment in individuals who have responded to ketamine, or (S)-ketamine, doesn’t have to be given on a daily basis.

“We can see that for instance with spravato [a nasal (S)-ketamine spray] and in many other regimens, where the frequency of dosing becomes lower and lower.” 

Ketamine without the trip

Ericsson says HMNC believes that its Ketabon formulation has a low likelihood of causing clinically significant dissociative side effects. 

Currently, whether or not the “trip” aspect of psychedelic therapy, and ketamine therapy, is necessary for clinical benefits is being debated. 

“For the dissociative effects of ketamine, I actually don’t think it’s absolutely needed,” said Eriksson. “In our small study in Switzerland, it was indeed possible to get an efficacy signal without dissociation. And there is also some data from academic studies out there looking at oral administration that look pretty encouraging. 

“Our hypothesis is that with the dose we have chosen, we will get the antidepressant efficacy, but we will not get the dissociative side effects. In our study, under the Clinician Administered Dissociative States Scale, which is one of the standard scales to look at dissociation – a common side effect of ketamine – the high dose of our drug was similar to the placebo.

“It was placebo level dissociation and there were also no signs of blood pressure increase, which is another typical consequence of giving ketamine intravenously or giving (S)-ketamine as a nasal spray.”

The company is aiming to develop the medication as a take-at-home medicine to over come the current challenges faced when delivering ketamine treatment. With IV ketamine treatment causing strong dissociative effects – patients must be treated in-clinic and supervised by a medical professional for a number of hours.

“I think there are two consequences of not having dissociative side effects,” said Eriksson. “One is that it will be good for patients, because many patients really disliked the dissociative experiences and they are quite unpredictable as well. 

“On a practical level, it will change things because if you’re taking a medicine like intranasal (S)-ketamine, which is a good medicine, you need to come into a physician’s office of the hospital several times during the treatment, once per week, twice per week and so on, and you need to stay there for several hours. 

“It’s really a complex treatment compared to if you can take the medicine at home. Our take-at-home approach has the potential to become a game changer for ketamine treatment.

“When you take psychedelic medicines that necessitate lots of staff and a controlled setting, meaning they become limited to a more severe end of the spectrum, which I think is natural. 

“If it will be possible to develop this medicine to something that gives efficacy with a very benign tolerability profile, then there is the potential to as a next step, continue developing the medicine for a broader use in psychiatric disorders, not necessarily only the treatment-resistant disorders.”

As Ketabon is an oral medication, Ericsson says HMNC will likely run a full effect study to find out whether the uptake is influenced by the food a patient is eating. 

So far, HMCN has spoken to several regulatory agencies and is aiming to take its treatment to the US and Europe, with development programmes designed to be fit for purpose for each market. 

“We believe that ketamine is a good antidepressant and that we can use Ketabon’s pharmacokinetic properties to disentangle the beneficial antidepressant effects from sometimes disturbing dissociative and cardiac effects,” Said Eriksson.

“That opens up the potential for a broader use of the medicine.”

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Is connection key? How clinicians impact patient outcomes in psychedelic therapy

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A wealth of research is showing how psychedelic-assisted therapy holds promise for the treatment of mental health conditions such as depression, but what role does the therapist play in a patient’s outcome? A new study has suggested it may be a big one.

Psychedelics have piqued huge interest due to their effects on the brain. Research points to their ability to induce neuroplasticity in the brain as one of the key reasons they may help with conditions such as depression and anxiety.

However, set – the individual’s (or patient’s) mental state – and setting – the individual’s environment during a psychedelic experience – are hugely impactful on the outcome of these experiences.

In the traditional use of psychedelic medicines, shamans help to guide set and setting throughout the experience with singing, drumming and ritual. Today, in scientific research, trials, and in clinics, the clinician is essentially playing this role.

Senior author of a new study, Alan Davis, associate professor and director of the Center for Psychedelic Drug Research and Education in The Ohio State University College of Social Work, has highlighted that the impact of clinicians on patient outcomes is not new, with research consistently showing that a trusting relationship between patients and clinicians has been key to better outcomes. This concept is known as a “therapeutic alliance”.

Understanding the therapeutic alliance

To find out more about the impact of this therapeutic alliance in psychedelic therapy, researchers from Ohio State University College of Medicine analysed data from a clinical trial that investigated psilocybin-assisted psychotherapy for the treatment of major depressive disorder (MDD).

In the trial, participants received two doses of psilocybin and 11 hours of psychotherapy, completing a therapeutic alliance questionnaire afterward, which assessed the strength of the therapist-participant relationship.

Participants also completed questionnaires about any mystical and psychologically insightful experiences they had during the drug treatment sessions. In psychedelic research, the mystical experience has often been shown to be related to the continuing positive effects of this therapy.

The Ohio team looked at the depression outcomes alongside patient reports about their experiences with the medicines as well as their connection with their therapists.

They found that a stronger relationship between patient and clinician led to a better clinical outcome for the patient – with improved depression scores up to 12 months following the experience.

Lead author Adam Levin, a psychiatry and behavioral health resident at Ohio State University College of Medicine, stated: “What persisted the most was the connection between the therapeutic alliance and long-term outcomes, which indicates the importance of a strong relationship.”

Analysis results revealed that over time, the alliance score increased, and in fact demonstrated more acute mystical experiences for the patient. The team also found that acute effects were linked to lower depression four weeks following treatment, but were not associated with better depression outcomes a year after the trial.

“The mystical experience, which is something that is most often reported as related to outcome, was not related to the depression scores at 12 months,” Davis stated.

“We’re not saying this means acute effects aren’t important – psychological insight was still predictive of improvement in the long term. But this does start to situate the importance and meaning of the therapeutic alliance alongside these more well-established effects that people talk about.”

According to the team, the analysis showed that a stronger relationship during the final therapy preparation session predicted a more mystical and psychologically insightful experience – which in turn was linked to further strengthening the therapeutic alliance.

“That’s why I think the relationship has been shown to be impactful in this analysis – because, really, the whole intervention is designed for us to establish the trust and rapport that’s needed for someone to go into an alternative consciousness safely,” Davis stated.

“This isn’t a case where we should try to fit psychedelics into the existing psychiatric paradigm – I think the paradigm should expand to include what we’re learning from psychedelics,” Levin added.

“Our concern is that any effort to minimise therapeutic support could lead to safety concerns or adverse events. And what we showed in this study is evidence for the importance of the alliance in not just preventing those types of events, but also in optimizing therapeutic outcomes.”

The authors emphasised that efforts to minimise negative experiences in future studies of psychedelics is vital, and that therapy is critical to creating a supportive environment for patients.

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Phase 2a trial to investigate 5-MeO-DMT candidate for alcohol use disorder

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Beckley Psytech and Clerkenwell Health are collaborating on a Phase 2a trial investigating Beckley’s synthetic 5-MeO-DMT candidate combined with psychological support as a treatment for alcohol use disorder (AUD).

AUD is estimated to affect around 237 million people across the globe and over 7.5 million people in the UK.

Treatment options for the harmful use of alcohol are not always effective – there are high relapse rates and there are around three million deaths each year attributed to the substance’s misuse.

Increasing research is showing that psychedelics may hold promise as innovative treatments for addiction, including substances such as ketamine and psilocybin.

See also  How psychedelics could help those living with alcohol use disorders

BPL-003 is Beckley Psytech’s short-duration and fast-acting synthetic formulation of 5-MeO-DMT – a psychedelic found in several plant species and the glands of at least one toad species – which is administered intranasally via an FDA-approved delivery device.

The compound has shown in Phase I data to be well-tolerated with a reproducible and dose-linear pharmacokinetic profile.

The Phase 2a trial

Beckley and Clerkenwell have confirmed that the collaborative Phase 2a open-label trial will evaluate the safety, tolerability and pharmacodynamic effects of a single dose of Beckley BPL-003 combined with abstinence-oriented psychological support in participants with AUD.

Currently taking place at King’s College London, Clerkenwell Health’s clinic near Harley Street, London, will provide an additional trial site.

According to Beckley, BPL-003 has been successful in eliciting psychedelic experiences of “similar intensity but shorter duration than psilocybin”.

Dr Henry Fisher, Chief Scientific Officer at Clerkenwell Health, stated: “An estimated 600,000 people are dependent on alcohol in England. This, coupled with an alarming increase in alcohol-related deaths of 89% over the past 20 years, shows the status quo isn’t working.

“Conventional treatments for alcohol dependency aren’t producing meaningful improvements and new avenues must be explored. This trial will assess whether psychedelic-assisted treatment can be an effective therapy for alcohol use disorder, with the hope of rolling out the treatment widely.

“Health professionals and policymakers should seriously consider such treatments, which could be genuinely ground-breaking for the NHS and for the hundreds of thousands of people being treated for alcohol use disorder in the UK.”

Beckley Psytech and Clerkenwell have emphasised that the results of the trial may be used to provide support for further study of psychedelic-assisted treatment for alcohol dependency.

Dr Rob Conley, Chief Medical and Scientific Officer at Beckley Psytech, added: “We’re committed to developing a transformative and effective treatment option for individuals struggling with alcohol use disorder.

“Based on our preclinical and Phase I data, we are optimistic about the potential therapeutic benefits of BPL-003 for substance use disorders and we are excited to evaluate the compound further in this clinical trial.

“I want to extend my thanks to the team at Clerkenwell Health and King’s, as well as to the patients who have joined, and will join, this study. Their participation, support and collaboration are absolutely critical to furthering research into this area of huge unmet need.”

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The Entourage Effect in Mushrooms: Natural psilocybin may outperform synthetic

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The Entourage Effect in Mushrooms: Natural psilocybin may outperform synthetic

A new study from the Hebrew University-Hadassah Medical Center has indicated that natural psilocybin extracts may demonstrate superior efficacy to synthetic psilocybin extracts.

Recent years have seen a boom in research into psilocybin for the treatment of mental health conditions such as anxiety and depression.

Many of the clinical trials investigating psilocybin use synthetic extracts rather than natural ones. This is because synthetic extracts will contain psilocybin alone, whereas natural psilocybe mushroom extracts will contain several different compounds such as psilocybin, psilocin, baeocystin and norbaeocystin.

Having multiple compounds can pose a challenge when running clinical trials as identifying which compounds are active and what their impact is becomes difficult to measure, and the concentrations of these compounds can vary depending on factors such as growth conditions and processing techniques.

This makes the standardisation of multi-compound medicines a huge challenge, as medicine consistency, reproducibility and dosing become difficult. However, these are essential factors when it comes to conducting clinical trials and receiving approval for medicines from regulators.

The Entourage Effect

In 2011 Dr Ethan Russo put forward the theory of the Entourage Effect in cannabis. 

The cannabis plant contains over 400 different cannabinoids that have so far been identified, such as THC, CBD, CBN and CBG.

Russo hypothesised that these different cannabinoid compounds work synergistically to create a therapeutic effect, as opposed to compounds such as THC or CBD working in isolation.

This hypothesis has been touched on only a few times in the scientific literature in relation to psychedelic mushrooms.

For example, in Dr Jochen Gartz’s 1989 paper ‘Biotransformation of tryptamine derivatives in mycelial cultures of Psilocybe’ which proposed a synergistic relationship between compounds in the mushrooms, and a 2015 paper by Zhuck et al, ‘Research on Acute Toxicity and the Behavioral Effects of Methanolic Extract from Psilocybin Mushrooms and Psilocin in Mice’, which observed that the effect of psychedelic mushroom extracts on mice was much stronger than pure psilocybin.

There has been very limited research on this hypothesis in mushrooms since. 

A new study: Natural may outperform synthetic

Now, a research team from Hebrew University-Hadassah Medical Center BrainLabs Center for the Psychedelic Research have compared a natural psilocybin extract to a chemically synthesised version.

Published in Molecular Psychiatry, results from the study indicate that the natural extract increased the levels of synaptic proteins associated with neuroplasticity in key brain regions, including the frontal cortex, hippocampus, amygdala, and striatum.

The ability of psilocybin to induce neuralplasticity has been indicated as one of the key features that contribute to its therapeutic effects.

The researchers suggest that these new study results indicate that nautral psilocybin extracts may offer unique therapeutic effects that may not be not achievable with synthesised, single-compound psilocybin alone. 

Metabolomic analyses also revealed that the natural extract exhibited a distinct metabolic profile associated with oxidative stress and energy production pathways.

The researchers write: “In Western medicine, there has historically been a preference for isolating active compounds rather than utilising extracts, primarily for the sake of gaining better control over dosages and anticipating known effects during treatment. The challenge with working with extracts lay in the inability, in the past, to consistently produce the exact product with a consistent compound profile. 

“Contrastingly, ancient medicinal practices, particularly those attributing therapeutic benefits to psychedelic medicine, embraced the use of extracts or entire products, such as consuming the entire mushroom. Although Western medicine has long recognised the “entourage” effect associated with whole extracts, the significance of this approach has gained recent prominence.”

However, compared to cannabis, the researchers suggest that mushroom extracts present a unique case, as they are highly influenced by their growing environment such as substrate, light exposure temperature and more.

“Despite these influences, controlled cultivation allows for the taming of mushrooms, enabling the production of a replicable extract,” the team writes.

The researchers emphasise that this research underscores the superiority of extracts with diverse compounds, and also highlights the feasibility of incorporating them into Western medicine due to the controlled nature of mushroom cultivation.

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Psychedelic Health is a journalist-led news site. Any views expressed by interviewees or commentators do not reflect our own. We do not provide medical advice or promote the personal use of psychedelic compounds. Please seek professional medical advice if you are concerned about any of the issues raised.

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