Innovations in paediatric medicines delivery awarded UnitaidExplore funding

  • Two new awards announced under Unitaid’s agility mechanism, UnitaidExplore; DelSiTech and FluidPharma will each receive investment for innovations to make medicines easier to give to children 
  • Latest call comes in context of Unitaid’s ground-breaking work on paediatric formulations to treat HIV, TB and malaria  
  • Children in low- and middle-income countries have lower treatment coverage and worse health outcomes than adults – a lack of paediatric formulations is a major contributing factor. 

Geneva, 4 October 2021Two companies developing potentially game-changing medicine delivery mechanisms for children are the latest recipients of UnitaidExplore funding. 

Finnish company DelSiTech and British enterprise FluidPharma have each been awarded funding following the latest call for applications under Unitaid’s pioneering agility mechanism.  

Children in low- and middle-income countries have lower treatment coverage and worse health outcomes than adults. A major barrier is a lack of medication that is specifically formulated for their needs. Often medicine is too bitter, difficult to swallow or not correctly dosed, making it hard for children to stay on treatment for diseases such as HIV, malaria and TB.  

The latest UnitaidExplore call specifically targeted this issue, inviting applicants to apply for funding to push forward innovation in this field. It builds on Unitaid’s significant work in the field of paediatric formulations for HIV, TB and malaria treatments, and its key role in WHO’s GAP-f network.

FluidPharma will use UnitaidExplore funding to take forward development of their MicroCoat™ technology, which utilises tiny cellulose spheres with taste-masking properties to deliver medication in a formulation that is more palatable to children. It is hoped that this technology could be used across a range of disease areas, with initial development of an artesunate/amodiaquine malaria combination therapy. 

DelSiTech’s work focuses on the development of long-acting injectables to deliver medicines to children, reducing the burden of tablets and the associated stigma with taking such medication. The technology involves the use of thin, minimally invasive needles to deliver a unique silica-based formulation via sub-cutaneous injection. The technology can be used to administer drugs that treat or prevent a wide range of conditions, while significantly extending the effective duration of the treatment from a single dose. 

Unitaid Director of Strategy Janet Ginnard said: “Innovations in medicine delivery that are specifically aimed at children are of utmost importance and we are pleased to announce this funding to DelSiTech and FluidPharma. These investments fit firmly with Unitaid’s track record in facilitating access to the best medicines for the most vulnerable people. These innovations will help ensure that children can benefit from lifesaving treatment and have the best possible health outcomes.” 

The investments from Unitaid will accelerate both companies’ paediatric delivery mechanisms, covering pre-clinical work for several different potential applications. 

Professor John Reeder from WHO’s GAP-f network said: “Unitaid’s new investments in innovative delivery approaches for children are extremely welcome, as they spark new energy and collaborations to ensure that science and innovation are at the service of those who have been too often left behind, our children.” 

Dr. Lasse Leino, Chief Executive Officer from DelSiTech said: “Alliances, such as with Unitaid, are essential to us and to healthcare organisations around the world for the realisation of our common goal, securing real advancements in global health. DelSiTech is committed to pursuing long lasting strategic partnerships, enabling us to play a role in improving treatment outcomes, now for clearly underserved children. We are thrilled to collaborate with Unitaid and are prepared to leverage the full extent of our technologies and expertise for paediatric solutions for patients, wherever they may be”. 

Dr Fang Liu from Fluid Pharma said: “We are really excited for this opportunity to join Unitaid’s excellent work in making medicines suitable for children. Applying the MicroCoatTM technology, we will develop paediatric anti-malarial treatments that are palatable, easy to swallow and stable, to improve compliance and treatment outcomes for children.” 

This announcement complements two awards given last year to the first UnitaidExplore recipients, Vayu Global Health and EPFL EssentialTech, to take forward innovations in paediatric oxygen delivery.


About Unitaid
Unitaid is a global health agency engaged in finding innovative solutions to prevent, diagnose, and treat diseases more quickly, cheaply, and effectively, in low- and middle-income countries. Its work includes funding initiatives to address major diseases such as HIV/AIDS, malaria, and tuberculosis, as well as HIV co-infections and co-morbidities such as cervical cancer and hepatitis C, and cross-cutting areas, such as fever management. Unitaid is now applying its expertise to address challenges in advancing new therapies and diagnostics for the COVID-19 pandemic, serving as a key member of the Access to COVID-19 Tools (ACT) Accelerator. Unitaid is hosted by the World Health Organization.


Media contacts

For more information and media requests:

 

Hervé Verhoosel

Head of Communications

Unitaid, Geneva

verhooselh@unitaid.who.int

tel. +44 77 29 618 634

 

Maggie Zander

Communication Officer

Unitaid, Geneva

zanderm@unitaid.who.int

tel. +41 79 593 17 74

Digital technologies support patients with treatment from a distance, allowing more flexibility in care

Research begins into new digital tools to support patients and healthcare workers through tuberculosis treatment

The Hague / Geneva, 4 August 2021A large global study which aims to determine if digital adherence technologies (DATs) can provide more patient-friendly approaches to improve tuberculosis (TB) treatment outcomes launches in Ethiopia, Tanzania, South Africa, the Philippines and Ukraine, as part of the ASCENT project.

The digital adherence technologies studied include medication labels and sleeves, smart pill boxes and video supported treatment that allow for remote communication between patients and healthcare centers.

These technologies respond to a key challenge in TB treatment: treatment is long and difficult to complete, lasting anywhere from six months to two years. Because of this, public health strategies have historically relied on Directly Observed Therapy (DOT), in which a clinician observes a patient taking their medicine each day to ensure adherence. These technologies aim to reduce or remove regular in-person visits required under the DOT model and enable healthcare workers to intervene only when necessary.

After COVID-19, TB is the deadliest infectious disease in the world, leading to 1.5 million deaths every year, despite being a curable disease.

The technologies are expected to improve experiences for TB patients and increase treatment completion rates by removing the heavy logistical, financial and time burdens that DOT places on both patients and health systems. Additionally, removing the need for DOT would make TB care significantly more efficient and represent huge savings to public health programmes.

The main research phase, now launched in all countries, evaluates three digital adherence technologies:

  • Smart pillboxes that send a message to the clinic every time the patient opens it up to take their medicine.
  • Medication labels or sleeves that help patients to send a code via SMS  to the clinic every time they take their dose.
  • A video application that helps patients film themselves taking their medicine, and then securely sends the video to the clinic.

 

Wide reaching applications

ASCENT aims to enroll thousands of TB patients by the end of 2022. If proven effective, these tools could have wide-reaching applications to support patients undergoing treatment for any disease which requires them to take medication over an extended period.

“Practical, patient-centered solutions are essential in developing public health strategies that work. Digital adherence technologies are designed to support people in taking their medication while providing information that helps healthcare workers give more tailored care. These innovations, when coupled with advances in treatment and prevention, could modernize and accelerate global efforts against TB,” said Janet Ginnard, Director of Strategy at Unitaid, global health agency and funder of the ASCENT project.

 

Research phase

ASCENT facilitates adoption and uptake of DATs in the five project countries in partnership with the national TB programs. The research component generates evidence for the proper use and scale-up of these innovations. The results are expected to offer guidance to the World Health Organization (WHO) and national TB programs.

We are trying to effectively evaluate whether health facilities that utilize DATs do better in terms of treatment outcomes than facilities that do not and why. We are also focused on understanding the acceptability of DAT and the social and financial benefits to both the patients and the health facilities,” said Jens Levy, chief researcher of the ASCENT project at the KNCV Tuberculosis Foundation.

In the Philippines, Ukraine, Tanzania and South Africa treatment outcomes will be reviewed during the six months of treatment. In Ethiopia the study includes a six-month follow-up beyond treatment to see if there is recurrence of TB. Study protocols are nearly identical in each country, allowing researchers to evaluate the effectiveness of DATs in a variety of healthcare settings and circumstances.

 

TB policy

For everyone working with these interventions and for those who want to in the future, scientific evidence is crucial. We are honored to lead this research. Contributing to the fight against TB in a patient friendly way”, said Mustapha Gidado, executive director of the KNCV Tuberculosis Foundation.

“If it’s shown to be a successful intervention, this could be very beneficial for worldwide TB programmes. It could also change TB treatment policy around the world,” said Katherine Fielding of the London School of Hygiene and Tropical Medicine, who is the co-investigator of the overall project and chief investigator for the Ethiopian study.

The Unitaid-funded and supported ASCENT project is led by the KNCV Tuberculosis Foundation (KNCV) in partnership with the Aurum Institute, the London School of Hygiene & Tropical Medicine (LSHTM), and PATH.


About the ASCENT project

The Unitaid-funded ASCENT project aims to help patients succeed in TB treatment using digital adherence technology, towards reducing TB incidence, mortality and financial consequences.

 

About Unitaid
Unitaid is a global health agency engaged in finding innovative solutions to prevent, diagnose, and treat diseases more quickly, cheaply, and effectively, in low- and middle-income countries. Its work includes funding initiatives to address major diseases such as HIV/AIDS, malaria, and tuberculosis, as well as HIV co-infections and co-morbidities such as cervical cancer and hepatitis C, and cross-cutting areas, such as fever management. Unitaid is now applying its expertise to address challenges in advancing new therapies and diagnostics for the COVID-19 pandemic, serving as a key member of the Access to COVID-19 Tools (ACT) Accelerator. Unitaid is hosted by the World Health Organization.


Media contacts

For more information and media requests

 

KNCV Tuberculosis Foundation

Laura Goense, Campaign and Media Manager

+31 (0)613 913 577

Laura.goense@kncvtbc.org

 

Unitaid

Hervé Verhoosel, Director, External Relations and Communication a.i.

+44 77 29 618 634

verhooselh@unitaid.who.int

Unitaid reaffirms its commitment to combat tuberculosis in times of COVID-19

Geneva – On World Tuberculosis Day 2021, Unitaid renews its strong commitment to fight one the world’s deadliest infectious killers.

Ensuring wider access to better, simpler and more affordable solutions to stop the spread of tuberculosis (TB) has always been at the core of Unitaid’s mission. While the world has come together to combat the COVID-19 pandemic, it is now more important than ever to redouble our efforts when it comes to TB.

Every year, about 1.4 million die from TB and 10 million people fall ill with the disease. The COVID-19 pandemic has intensified existing access challenges to efficient prevention, diagnosis and care, threatening to reverse the gains made over recent years.

Disruptions in TB services, diversion of resources and substantial reductions in TB detection have been observed. Between 2020 and 2025, an additional 1.4 million TB deaths could be registered as direct consequence of the pandemic.

Urgent action must be taken to provide wider access to life-saving preventive tools, tests and treatments if we want to reach our objective of ending TB by 2030.

“In these exceptional times, innovation has proven to be even more critical than ever to tackle tuberculosis. We need to redouble our efforts across prevention, diagnosis and treatment to ensure that affordable, simpler and adapted solutions are made available in low- and middle-income countries, particularly for the people who need them the most” said Dr Philippe Duneton, Unitaid Executive Director.

Working closely with strategic partners, Unitaid has been at the forefront of investing in cutting-edge innovative solutions. Those include better treatments for children, better regimens to tackle multi-drug resistant TB, more accurate diagnostics to detect cases, shorter, more affordable regimens for TB prevention and digital technologies to help patients stick to their treatments.

Unitaid’s TB portfolio has nearly doubled over the past two years reaching about US$ 250 million. In 2020, the organization was ranked as one of the world’s largest multilateral funder in TB research and development and first for pediatric TB research.

Unitaid’s work in TB:


Media contact: Maggie Zander | +41 79 593 17 74 | zanderm@unitaid.who.int

Unitaid looks to invest in better tools to improve tuberculosis detection

Geneva – Unitaid is pleased to announce a new call for proposals in the area of tools to drive tuberculosis (TB) detection.

Despite recent advances in the fight against TB, progress is not sufficient to reach global goals. According to the 2020 WHO Global TB Report, nearly 1.4 million people died from TB in 2019. Of the estimated 10 million people who developed TB that year, about 3 million were either not diagnosed, or not officially reported to national authorities. TB continues to be one of the deadliest infectious disease in the world, especially for the most vulnerable. In spite of the recent advancements in treatment and diagnosis, existing tools are inadequate and/or underutilized to close the gap in identifying missing cases.

In addition, the COVID-19 pandemic has started to undo progress made to date. There are major disruptions to TB programs and supply chains and substantial reductions in numbers of individuals being diagnosed and seeking care.

In this context, there is a need for rapid diagnostic tools that can test for many pathogens and be implemented in primary healthcare settings including local health clinics, medical offices, health posts, or by community health workers during home visits.

Without substantial intervention to address the gap in finding missing TB cases, TB transmission will remain out of control, perpetuating the TB epidemic, leading to continued morbidity and mortality.

Under this call, Unitaid is soliciting proposals that aim to bring innovative diagnostic solutions to ensure that a person with TB receives timely, reliable diagnosis that links with referral to appropriate care, thereby saving lives and contributing to achieving the global targets for ending the TB epidemic.

The closing date for receipt of full proposals is Monday 24 May 2021 at 12:00 (noon) CET.  


About Unitaid calls for proposals

Through calls for proposals, Unitaid finds partners best qualified to put key innovations into practice. A review committee of independent experts in global health helps choose the best proposals to fund through a competitive selection process. Partners receive grants from us to fast-track access and reduce the costs of more effective medicines, technologies and systems. In this way, Unitaid’s investments establish the viability of health innovations, allowing partner organisations to make them widely available.


Media contact: Maggie Zander | +41 79 593 17 74 | zanderm@unitaid.who.int

New patient-friendly tuberculosis preventive treatment to be rolled out in five high-burden TB countries at affordable price

  • Fixed-dose combination treatments reduce the pill burden from nine to three pills a week for adults and prevent TB in those at highest risk of developing the disease 
  • Ethiopia, Ghana, Kenya, Mozambique, and Zimbabwe will be the first countries out of a total of 12 to provide the new regimen at a US$15 price thanks to funding from Unitaid, PEPFAR and the Global Fund to Fight AIDS, Tuberculosis and Malaria 

Johannesburg — A new fixed-dose combination (FDC) of “3HP”, a short-course tuberculosis (TB) preventive treatment (TPT) combining two drugs, rifapentine and isoniazid, is starting to be rolled out in five TB high burden countries in Africa. This will reduce the number of pills that people who need the treatment have to take every week from nine to three. Enough treatments for up to 3 million patients are expected to be made available for eligible countries this year.

As the result of an agreement concluded by Unitaid, the Clinton Health Access Initiative (CHAI) and the manufacturer of the FDC, Macleods, the latter has agreed to offer a ceiling price of US$15 (ex works) for a three-month patient course of weekly rifapentine and isoniazid. Thanks to the IMPAACT4TB project funded by Unitaid and led by the Aurum Institute, five initial countries from a total of 12 targeted by the end of the year, will start providing the FDCs in February and March 2021: Ethiopia, Ghana, Kenya, Mozambique, and Zimbabwe. Other countries are expected to receive supplies with the support of PEPFAR and the Global Fund to Fight HIV, Tuberculosis and Malaria.

The partnership with Macleods will bolster efforts to treat TB infection also known as “latent TB” – currently estimated to affect one quarter of the world population – by broadening access to shorter and easier to use preventive therapies. As part of a wider access strategy to facilitate the introduction of generic rifapentine-based formulations in low- and middle-income countries (LMICs), it will contribute to move towards the United Nations High-level Meeting (HLM) target to provide TPT to at least 30 million people by 2022.

“WHO welcomes the new fixed-dose combination TB preventive treatment that will result in reducing the pill burden for people with TB infection, enabling better adherence and outcomes,” said Dr Tereza Kasaeva, Director of World Health Organization’s (WHO) Global TB Programme. “This collaboration between Unitaid, the Clinton Health Access Initiative and manufacturers has been vital to support the uptake of TB preventive treatment as recommended in WHO guidelines. We now look forward to a surge in action from national programmes supported by donors and partners to scale-up access to TB preventive treatment and reach the UN High-Level Meeting targets.”

People with TB infection, often dubbed latent, have no symptoms, are not contagious and most do not know they are infected. Without treatment, 5% to 10% of these people will develop active TB, the form which makes people sick and can be transmitted from person to person.

The agreement establishing the US$15 price and other access conditions was concluded by Unitaid, the Clinton Health Access Initiative (CHAI) and Macleods. The price will be available to government institutions in 138 LMICs, as well as for the international organizations in charge of the procurement.

“The ceiling price agreement negotiated with Macleods is another example of our commitment to ensure that effective, quality-assured and affordable TB preventive therapies are made available in low- and middle-income countries,” said Robert Matiru, Director of the Programme Division at Unitaid. “Beyond this deal, we will continue working hard to ensure a healthy market for all manufacturers that wish to develop and commercialize rifapentine-based products.”

The first phase of the access strategy resulted in a price discount offer by Sanofi for rifapentine 150 milligram tablets (Priftin®), announced in 2019, lowering a patient treatment course of Priftin® from US$45 to US$15.

“The availability of a shorter, more easily tolerated, and safer regimen for TB prevention that is also affordable is critical for accelerating the fight against TB,” said Dr. Angeli Achrekar, Acting U.S. Global AIDS Coordinator. “This also has important implications for the HIV response, as TB remains the leading cause of death for people with HIV around the world.”

With both Sanofi and Macleods expected to ramp up their production in 2021, Unitaid expects that there will be global availability of enough 3HP to reach more than 3 million patients in eligible countries this year, across both manufacturers.

“2020 was a hard year for TB prevention and treatment, as many services were disrupted by lockdowns,” said Prof. Gavin Churchyard, founder and CEO of the Aurum Institute. “But with the roll-out of this new FDC, alongside the existing formulation provided by Sanofi, I’m feeling a renewed sense of optimism that we can get back on track to meet our ambitious global TB prevention goals. Saving lives is the priority. We lose in the end if COVID-19 mortality goes down, but TB rates go up.”

With the FDC, a complete course of treatment for eligible adults is included in one box, addressing many concerns about the pill burden of 3HP and ensuring that TPT can be provided conveniently for individuals at risk for TB.

With this more convenient product in hand that is easier to dispense, take and adhere to, the IMPAACT4TB consortium members are now working to accelerate the delivery of 3HP in 12 high TB burden countries in Africa, Asia, and South America.

For its part, USAID, the largest bilateral funder of TB efforts globally, has been a leader in partnering with high burden TB countries in the successful implementation of their national TB strategies for over 20 years. Preventive TB treatment is a cornerstone of USAID’s Global Accelerator to End TB, which builds countries’ commitment and capacity to reach the United Nations HLM TB targets by 2022. Having a shorter FDC TPT regimen available at a relatively low price will enable USAID to work with partners and stakeholders to rapidly scale up TPT for all who would benefit from it in high burden countries.


Additional quotes

“The availability of this new fixed-dose combination is good news for everyone, especially patients and their families,” said Ahmed Bedru, KNCV Tuberculosis Foundation country representative, leading 3HP implementation for Ethiopia. “Getting people to adhere to a treatment when they are not sick has always been a challenge. The lower number of pills — three pills versus nine pills for an adult — means the treatment is now easier to take, stick to and complete.”

“I’ve started to notice patients taking their medication without difficulties or complaints,” said Dr. Tafadzwa Priscilla Sibanda, Medical Director of the Mpilo Centre and a public health specialist working with the AIDS Healthcare Foundation in Zimbabwe. “It really helps that the 3HP regimen is short. When we explain the doses to patients, they can see the light at the end of the tunnel, and they are encouraged knowing that they will complete the course within 12 weeks.”

“Adherence is always a challenge, especially when people have to take many pills for long periods of time. But 3HP is changing that. The FDC allows patients to take just three pills once a week for 12 weeks. This will be so much better,” said Dr. Pereira Zindoga, a clinician with the Mozambique Ministry of Health’s  National TB Program.


About TB infection

In 2019 alone, 10 million people fell ill from TB, which killed close to 1.5 million people, over 95% of whom were living in low- and middle-income countries. About one quarter of the world’s population is infected with TB bacilli and the most of them do not have the disease and are not contagious. If left untreated, TB infection may progress to TB disease, the form of TB that makes people sick and is capable of being transmitted from one person to another. TPT regimens like 3HP lower the risk of progression in people at risk.

About 3HP: Using the FDC, the once-weekly dose over 12 weeks — a complete course of treatment for eligible adults — is contained in one box. This formulation addresses many concerns about the pill burden of 3HP and will ensure that TPT can be provided conveniently for programmes, providers and individuals at risk for TB. 3HP offers many benefits for infected individuals, clinicians and programs compared to the previous standard of care, when patients were required to take a pill daily for six months or more.

About IMPAACT4TB: Unitaid is investing US$59 million in the Aurum Institute’s IMPAACT4TB project, to protect people most vulnerable to developing active TB. IMPAACT4TB is led by the Aurum Institute in consortium with the Clinton Health Access Initiative, KNCV Tuberculosis Foundation and John Hopkins University, in collaboration with the World Health Organization (WHO) and the Global Drug Facility (GDF). The four-year grant will prioritize short-course TB preventive treatment for people living with HIV and children under five, and subsequently all those in close contact with TB patients in 12 high-burden countries. The target groups will receive a quality-assured, affordable, short-course TB preventive treatment known as 3HP, consisting of high-doses of two antibiotics that treat TB (isoniazid and rifapentine given weekly for three months). www.unitaid.org and www.impaact4tb.org

South Africa’s Aurum Institute is spearheading the TB prevention project and is working with the Clinton Health Access Initiative, KNCV Tuberculosis Foundation, and John Hopkins University, in collaboration with the World Health Organization and the Global Drug Facility.


Media contacts

Unitaid: Maggie Zander | +41 79 593 17 74 | zanderm@unitaid.who.int

The Aurum Institute: Kanya Ndaki | +27 832986100 | KNdaki@auruminstitute.org

Unitaid funding sees launch of world’s first long-acting medicines centre at University of Liverpool

Geneva – Efforts to revolutionise treatments for debilitating infectious diseases have been amplified today with the launch of a new research centre at the University of Liverpool.

Established as part of a US$40 million international research consortium, primarily funded by Unitaid, the University of Liverpool’s Centre of Excellence for Long-acting Therapeutics (CELT) will be the first of its kind in the world.

By repurposing existing medicines into slow-release formulations, where drug effectiveness can be sustained over several months, ‘long-acting’ technology has already been successfully implemented in the fields of contraception and schizophrenia.

It now has the potential to improve the outcomes for treatment and prevention of deadly diseases such as HIV, malaria, Hepatitis C and tuberculosis, which particularly impact low- and middle-income countries.

Current treatment courses for these conditions have often resulted in poor outcomes in low-resource environments, as those living with diseases struggle with regimens that can involve taking dozens of tablets every day and rely on regular access to healthcare settings.

CELT’s mission is to broaden knowledge of long-acting medicines and disseminate key research, with the aim of revolutionising how these devastating diseases are treated, particularly in countries where access to healthcare is challenging.

The work will be conducted out of two state-of-the-art laboratories at the University of Liverpool, where the development of long-acting formulations for malaria and TB prevention, as well as a single-injection cure for hepatitis C, is already under way as part of the Unitaid-funded LONGEVITY project. In the case of malaria prevention, for example, the aim is to cover an individual for the entire malaria season with just one injection.

Meanwhile, by facilitating collaboration between scientists from the fields of pharmacology and materials chemistry, as well as global partners, CELT will ensure that the long-acting medicines are carefully designed with the specific needs of affected communities in mind.

Other projects focus on helping researchers understand better the key success factors for oral, injectable and implantable long-acting approaches.

Unitaid’s Executive Director Dr Philippe Duneton said: “Decades ago, long-acting products revolutionised fields such as schizophrenia and contraception. Today, our goal is to apply similar innovation to bolster global efforts to tackle – and even eliminate – major diseases affecting low- and middle-income countries, including HIV/AIDS. The pipeline of new long-acting products is promising. As a funder of catalytic health interventions, we are excited and inspired to be supporting the University of Liverpool, and other partners, that are blazing a trail in that regard.”

Co-director of CELT, Professor Andrew Owen, said: “Long-acting drug delivery promises to transform patient management, with huge potential impact for treatment and prevention of infectious diseases. Benefits for efficacy flow from overcoming issues associated with patients sometimes not taking their medication, which may also help reduce emergence of antimicrobial resistance. CELT harnesses the power of local, national and international collaboration to accelerate understanding of the medicines of the future.”


Media contact: Charlotte Baker | +44 7904 460 181 | bakerc@unitaid.who.int

How digital technologies can empower patients to succeed in TB treatment

How digital technologies can empower patients to succeed in TB treatment