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Clerkenwell Health: Developing a gold standard for psychedelic care

Clerkenwell Health is aiming to accelerate the development of efficacy data and help deliver psychedelic clinical trials at speed and scale.

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UK sees crossparty call to review scheduling of psilocybin

UK company Clerkenwell Health is working to develop a gold standard in the delivery of psychedelic care.

Clinical trial company Clerkenwell Health is embarking on institutional partnerships to conduct psychedelic research and drug development, helping psychedelic compound manufacturers commercialise their products. The company is also building the first custom-designed Centre of Excellence for psychedelic clinical trials.

By focusing its research on the benefits of therapy alongside supportive technologies, Clerkenwell aims to create a best-in-class, regulatory approved framework for delivering psychedelic-assisted psychotherapy. 

Clerkenwell CEO Tom McDonald and CSO Dr Henry Fisher spoke to Psychedelic Health about its plans to accelerate the development of efficacy data and help deliver psychedelic clinical trials at speed and scale.

Set and setting for optimal patient outcomes

Clerkenwell is setting up its Centre of Excellence in 2022,  which will be built with set and setting in mind – aiming to create beautiful spaces that will optimise outcomes for patients. 

McDonald commented: “There has been a bit of a shift over the past 15 to 20 years towards more speciality clinical research outfits and we think psychedelics, in particular, are really relevant for this. 

“Typically, trials at the moment – be they for oncology or viruses, or now, psychedelics and mental health – they are typically taking place in pretty unpleasant looking environments. So, out of the back of a university hospital is really the option that companies have got here in the UK at the moment. 

See also  Partnership to advance patient access to psychedelics in Europe

“We will be creating a really beautiful setting – more akin to the priory than a university hospital – out in a nice remote place. The rooms will be designed specifically to be conducive to a positive psychedelic experience that might therefore get incremental gains in the outcomes that the patients are going to receive.

“This is what is needed to drive the industry forward. We have also got an ambitious scale-up process that will go hand in hand with our partners’ drug development, as they are looking to increase the number of sites and then potentially increase the number of countries as well.”

Best-in-class psychedelic therapy training

Clerkenwell is working with The University of Manchester to design its own study exploring the therapy component of psilocybin depression treatment.

The team aims to build a best-in-class, accredited therapist training programme aligned with regulation, working closely with Dr Sara Tai, a senior lecturer in clinical psychology at the University of Manchester. Dr Tai, who previously helped design the therapist training programme for COMPASS Pathways, focuses her research on the similarities and differences between types of therapy. 

“We think there is a real uniqueness to psychedelics – unlike any other drugs really in the history of them, the talking therapy component is so important for the vast majority of these conditions,” said McDonald.

“So, by building expertise in understanding what therapy works, working across a range of different psychedelic compounds and a range of different conditions, we are going to be able to build a real best-in-class, therapist training programme that is closely aligned to what the regulators know and understand, and we will look to get that accredited by a serious body.

“There are still a lot of unknowns around the therapy component of these treatments, so we were looking to do some really interesting bits looking at depression – but specifically drilling into the therapy component and what digital therapeutics could be doing to help support the patient in addition to that.”

Fisher commented: “What we are very conscious of is the data on what types of therapy work and how the different types might benefit different people – interrogating how we can optimise the therapy for patients and optimise technology that sits alongside it to support the sustained efficacy of treatment. 

“I think one of the key things that may come out of some of the other trials that have been conducted is that it might be hugely effective in the short to medium-term, but actually if there is not ongoing support – just as with therapy without psychedelics – actually, depression can creep back in.”

Supporting the development of psychedelic care

Clerkenwell is currently working with Octarine Bio, which is which using yeast fermentation to produce psilocybin from sugar, to design clinical trials. 

“They’ve been working with the biosynthesis of various different compounds, they started with cannabinoids and now are looking to develop psilocybin as their first entity but potentially others down the line as well,” said McDonald. 

“We will provide everything from very early stage clinical advisory services, helping them design the study that they want to run, and then actually operationalising that when our site is ready in quarter two of next year. We are also likely to start engaging the regulators on their behalf in the not too distant future.”

In its partnership with Octarine, Clerkenwell has been epxloring conditions that have very poor treatment options available and identifying indications it believes psilocybin-assisted therapy is going to be beneficial for. 

“Octarine’s development is going to be more viable than the traditional lab development models, and also, when done at scale, is going to be considerably cheaper than others out there as well so, we are really hoping that helps with patient access – identifying a niche condition that has very poor treatment options and then providing a drug and this is associated therapy at a reasonable cost.

“When you start looking at the impact on quality of life or whether people are able to return to work and therefore get back into paying taxes, all of those downstream impacts are what we think is really interesting. Looking at some of those early-stage results where people are coming out after a single or two doses are at three months or potentially even six months are essentially symptom-free or heavily-reduced is where we think that there is real value.”

Fisher added: “The whole point of what we are trying to do is help companies that are want to bring these drugs to markets, build the data that is required to present to regulators, and do so in as an efficient and timely way as possible – being very conscious that either the current options either don’t have the correct facilities to be able to generate the best data. 

“Ultimately that will be the way that these drugs can get into patients hands as quickly as possible.

“I think something that Europe, but also the UK especially, has to their benefit here is that it has really strong research. Imperial College London and King’s College are world leaders in psychedelic research – since the start of the psychedelic renaissance. 

“That gives us a really strong basis on which to build collaborative research – there is a rich ecosystem of researchers that are keen to work with different people, and organisations that are just looking to push the whole sector forwards.

“We’re hoping to fit into that, where we can both work with the for-profit in the space and partner with other organisations and researchers, helping to deliver the trials that require input from different areas.”

Fisher, who started working in psychedelic research in 2015 at the Beckley Foundation, drug policy think tank, Volteface, The Loop, campaigning for drug reform, before founding Hanway Associates a cannabis sector advisory firm, continued: “It’s just wonderful to come full circle from where I started. I had a real passion for the potential of psychedelics years ago when it was only in the academic sphere. It didn’t look like this was anywhere near on the horizon. Now, it is very much reality. 

“It will be a paradigm shift when these drugs can actually be delivered to patients and it is very rewarding to be a part of that process.

“We are trying to focus on providing real gold standard, and paradigm-shifting care that we need to be doing in the trials to start with and then hoping that translates into real-world delivery. We are trying to help patients and get to the root cause, with the use of psychedelics in combination with therapy.”

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Markets & Industry

Major deals continue positive trajectory for psychedelics in 2024

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“Enhanced Consciousness Index” tracked by new psychedelics ETF

Psychedelics started 2024 with a bang, and the innovative medicines are continuing to gain traction as the year progresses. This week saw one of the globe’s top five biggest pharmaceutical companies – AbbVie – enter the market, while Enveric and MindBio signed a $66.5 million deal.

2024 set off to a strong start for psychedelic medicines with several watershed moments that are setting the stage for the sector’s acceleration.

These include developments such as the FDA’s acceptance of Lykos Therapeutics’ NDA for MDMA-assisted therapy for PTSD, Beckley Psytech’s securement of $50M investment from atai Life Sciences to expedite its assets through Phase 2 trials, a European Medicines Agency meeting on regulating psychedelics, and the confirmation from the UK’s independent policy body POST that it will publish a major briefing on psychedelic drugs to treat mental health conditions later this year, among others.

The positive developments for the industry are continuing, with this week seeing pharmaceutical company AbbVie – which has a clinical pipeline covering neuroscience, immunology, oncology, and eyecare – entering the industry through a new $65 million partnership with psychedelic drug developer Gilgamesh Pharmaceuticals.

Next generation neuroplastogens

The companies have stated they will be working together to discover and deliver next-generation psychedelics for mental health conditions such as anxiety, depression, and PTSD, as well as addiction.

AbbVie has highlighted the challenges posed by first-gen psychedelics including necessitating in-office administration and concomitant supportive care due to their hallucinogenic component – elements that could hinder the adoption and scale-up of these medicines.

See also  MDMA for PTSD receives priority review for New Drug Application

Gilgamesh Pharmaceuticals is working on the development of next-gen compounds that aim to improve the safety and efficacy of first-generation psychedelics and remove the hallucinogenic component, including a short-acting 5-HT2A agonist and an Ibogaine analogue.

In a press statement, Jonathon Sedgwick, Ph.D., senior vice president and global head of discovery research at AbbVie, commented: “Significant unmet need remains for people living with psychiatric disorders and we know that to innovate in this field, we need to pursue novel technologies and approaches.

See also  UK advisory body issues rapid response on psychedelics for PTSD

“We look forward to working with Gilgamesh’s world-class team to advance the development of novel neuroplastogens and pave the way for additional treatment approaches in psychiatry.”

Jonathan Sporn, M.D., chief executive officer at Gilgamesh Pharmaceuticals, added: “We are thrilled to partner with AbbVie, a global pharmaceutical company focused on innovation in psychiatric care, to address the pressing challenges in mental health treatment.

“Our collaboration will pioneer research of a new generation of therapies that hold great potential for improving patient outcomes.”

AbbVie is now the latest major pharmaceutical company to enter this market, following the likes of Janssen and Janssen and Otsuka Pharmaceutical, indicating that mainstream pharma is taking the promise of psychedelic medicines seriously.

However, this was not the only major deal to take place in the psychedelics market this week.

Enveric Biosciences also signed a $66.5 million non-binding term sheet with MindBio Therapeutics to out-license its novel psilocin prodrug candidate for mental health disorders.

Similar to Gilgamesh Pharmaceuticals, Enveric and MindBio focus on the development of next-generation neuroplastogens for that have reduced the hallucinogenic component.

Under the non-binding term sheet, Enveric will out-license a class of Novel Psilocin Prodrugs (NPP) to MindBio – a group of molecules that the company says are designed to be metabolised specifically to release therapeutic levels of systemic psilocin at varying rates.

In a press statement, Joseph Tucker, Ph.D., Director and CEO of Enveric, commented: “We look forward to working with MindBio’s team, which is pioneering an important part of the exciting psychedelic space, focused on controlling dose to reduce or eliminate hallucinations associated with these powerful compounds.

“This non-binding term sheet highlights the potential synergies between the Enveric and MindBio approaches to leveraging psychedelic-based compounds to target specific signaling pathways in the brain for the treatment of neuropsychiatric conditions.”

“We are pleased to explore an opportunity to draw on the molecular discovery engine at Enveric and believe this novel and patented asset significantly strengthens our intellectual property pipeline and aligns with our strategy to develop innovative, protected compounds with fine-tuned formulation and dosing strategies,” added CEO of MindBio, Justin Hanka.

“We look forward to the prospect of progressing this asset into clinical trials as we seek to bring important and beneficial therapies to patients in need.”

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Policy

UK advisory body issues rapid response on psychedelics for PTSD

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UK Government issues rapid response on psychedelic research

The UK’s independent Parliamentary Office of Science and Technology (POST) has issued a rapid response on psychedelic-assisted therapy for post traumatic stress disorder (PTSD).

The response is intended to inform policymakers on the topic as increasing research around psychedelics shows the compounds may hold promise as innovative treatments in the area of mental health.

The rapid response is the third response on psychedelics to come from POST – one of the first independent bodies of its kind in the world that sources independent analysis of public policy issues relating to science and tech for government.

Previous responses have covered depressive disorders, anxiety disorders and eating disorders.

See also  UK MPs demand answers as Drugs Minister dodges psilocybin debate

The response reads: “Research into the use of psychedelic-assisted psychotherapy for PTSD has been conducted using MDMA, ketamine, and the four ‘classical psychedelics’ (psilocybin, LSD, mescaline and DMT). These are described in POST’s rapid response article on depression.

“Generally, this approach involves ‘non-trip’ sessions with a medical professional to ensure safety, prepare the patient and build a relationship, and a minimum of one ‘trip’ session where the patient undergoes a form of talking therapy after administration of a psychedelic compound.

“Evidence from studies conducted in hundreds of participants suggests that psychedelic-assisted psychotherapy may be an effective treatment for PTSD. However, to date, there is not enough information from large clinical trials with sufficient participants comparing psychedelic-assisted psychotherapy directly to existing treatments.”

Responding to research and policy developments

POST’s responses on psychedelics have been issued following a parliamentary debate discussing psilocybin access in May 2023.

The debate saw a group of crossparty MPs call for the rescheduling of psilocybin to remove barriers to research and demand an urgent review of the evidence for psilocybin’s current status as a Schedule 1 drug under the Misuse of Drugs Regulations 2001, “with a view to rescheduling”.

The Royal College of Psychiatrists, psychedelic access non-profit Heroic Hearts UK, and other leading mental health charities, also wrote letters to the Veterans Minister and the Minister of State for Crime, Policing and Fire, urging them to champion access for patients in the UK.

The latest rapid response covers psychedelics for PTSD including Psychedelic-assisted psychotherapy for treating PTSD, MDMA, Ketamine, Classical Psychedelics and the Regulation of psychedelic drugs used in medicine.

Earlier this year, POST confirmed it intends to publish a major briefing on psychedelic drugs to treat mental health conditions in 2024.

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Research

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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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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