Micro Insurance Company Partners With Chamasure to Provide Digital Insurance Solutions in Kenya

NEW YORK, Oct. 20, 2021 (GLOBE NEWSWIRE) — MicroEnsure – now part of Micro Insurance Company (MIC) – has entered into a strategic partnership with Nairobi-based insurance platform Chamasure to give communities across Kenya access to digital insurance solutions. Chamasure makes insurance affordable for more than 10 million people in underserved communities in Kenya, including groups of farmers, traders, and families. Groups sign up via an easy-to-use app and are offered customized, flexible cover.

The new partnership between Chamasure and MIC will provide end-to-end enrollment, coverage, and claims settlement support, reducing paperwork for customers and speeding up the insurance process. Need-based cover will safeguard group members against disability, funeral costs, and medical expenses.

Ms Wairimu Nioki, Country Manager for MIC Kenya says:

“Communities have always come together to raise money to meet obligations that are too difficult for individuals to cover. We are now going to these communities and groups to simplify insurance for them by providing the protection that they seek when they come together. This initiative with Chamasure will see us providing more affordable insurance solutions and wider coverage, providing relief to members of these groups and consequently improving their lives.”

Speaking at the launch of the partnership, Seroney Memba, Chamasure Founder, said:

“Most of the people in the communities we work with have never had a chance to access insurance, despite being so vulnerable and in need of protection. We are excited to partner with Micro Insurance Company to provide these communities with more flexible, affordable products. Our motto is ‘taste insurance for everyone’, and I strongly believe this is the right partnership to achieve this.”

For more information, please contact:
Seroney Memba: seroney@chamasure.com
Wairimu Njoki: wairimu.njoki@microinsurance.com

About Micro Insurance Company (MIC):

Micro Insurance Company (MIC) is the world’s first end-to-end digital microinsurance platform that combines reinsurance capacity, in-country insurance licenses, world-class distribution, and market-leading AI functionality. Our global insurance platform delivers technology,underwriting, policy management, and distribution to platforms, micro and small businesses, and to the four billion people on the planet who are currently unserved. Whereas most insurtechs seek to improve existing monoline products and markets, we follow straight through processing to create highly relevant insurance products at a very low cost.

To find out more, visit https://microinsurance.com/

About Chamasure:

Chamasure, based in Nairobi, is an insurance platform that focuses on helping underserved communities, such as groups of traders and farmers, access affordable, customized insurance. Benefits include easy set-up, fast claims processing and payment, seamless mobile payments, and 24/7 app support. Groups who sign up to Chamasure have control of the full insurance process, from onboarding and peer vetting, to voting on claim validity and knowing when claims are paid.

To find out more, visit https://www.chamasure.com/

Adagio Therapeutics Divulga Novos Dados In Vitro Destacando a Neutralização Ampla e Potente do ADG20 Contra Todas as Variantes Conhecidas de SARS-CoV-2

Dados a serem apresentados na Conferência Virtual ISIRV-WHO 2021

WALTHAM, Mass., Oct. 19, 2021 (GLOBE NEWSWIRE) — A Adagio Therapeutics, Inc., (Nasdaq: ADGI) uma empresa biofarmacêutica de estágio clínico focada na descoberta, desenvolvimento e comercialização de soluções com base em anticorpos para doenças infecciosas com potencial pandêmico, divulgou hoje novos dados in vitro demonstrando a atividade neutralizante retida de seu anticorpo monoclonal (mAb), ADG20, contra um painel diversificado de variantes circulantes de SARS-CoV-2, incluindo as variantes Lambda e Mu recém-surgidas. Notavelmente, os resultados mostram que o ADG20 demonstrou atividade neutralizante in vitro potente contra todas as variantes preocupantes do SARS-CoV-2 testadas, incluindo as com suscetibilidade reduzida a produtos de mAb atualmente disponíveis sob Autorização de Uso de Emergência (EUA) ou em desenvolvimento em estágio final. Esses dados serão apresentados durante uma sessão de pôster na Conferência Virtual ISIRV-WHO 2021, a ser realizada de 19 a 21 de outubro de 2021. Além disso, a Adagio apresentará um cartaz do Encore destacando os dados recentemente publicados do teste em andamento da Fase 1 do ADG20 da empresa em participantes saudáveis.

“Esses novos dados de variantes ressaltam ainda mais o potencial do ADG20 para abordar a pandemia da COVID-19 em curso, bem como possíveis surtos futuros causados por outros vírus semelhantes ao SARS”, disse Laura Walker, Ph.D., cofundadora e diretora científica da Adagio. “Projetamos intencionalmente este mAb para ter atividade neutralizante ampla e potente, bem como uma meia-vida que estende sua janela potencial de proteção, características críticas que podem diferenciá-lo de outras terapias disponíveis nos EUA ou em desenvolvimento hoje. Com os testes globais de prevenção e tratamento da Fase 2/3 em andamento, estamos prontos para dar continuidade à nossa análise do ADG20 para avaliar o papel significativo que ele poderia ter no arsenal de opções de tratamento da COVID-19. Aplicado com uma única injeção intramuscular em ensaios clínicos, o ADG20 foi projetado para oferecer proteção durante até um ano no cenário de prevenção e está sendo explorado como um tratamento para pacientes de alto risco e/ou como um suplemento de vacina, inclusive para indivíduos imunocomprometidos.”

Além do estudo com participantes saudáveis de Fase 1, a Adagio está avançando dois estudos globais de Fase 2/3 em andamento com ADG20, um estudo de tratamento (SELO) e um estudo de prevenção (EVASÃO). A empresa prevê entrar com pedido de autorização do ADG20 na Food and Drug Administration dos EUA no primeiro trimestre de 2022.

Detalhes da Apresentação
Título do Cartaz:
 (130) Neutralização in vitro ampla e potente variantes de variantes do SARS-CoV-2 com o ADG20, um anticorpo monoclonal prolongado de meia-vida em desenvolvimento para a prevenção e tratamento da COVID-19

Título do Poster: (131) Avaliação da segurança, tolerabilidade e farmacocinética do ADG20, um anticorpo monoclonal prolongado de meia-vida (mAb) em desenvolvimento para a prevenção e tratamento da COVID-19: uma análise preliminar de um estudo randomizado de fase 1

Sobre o ADG20
O ADG20, um anticorpo monoclonal direcionado à proteína Spike do SARS-CoV-2 e coronavírus relacionados, está sendo desenvolvido para a prevenção e tratamento da COVID-19, a doença causada pelo SARS-CoV-2. ADG20 foi projetado e criado para alta potência e ampla neutralização contra SARS-CoV-2 e sarbecovírus de clado 1 adicionais, direcionando-se a um epítopo altamente conservado no domínio de ligação ao receptor. O ADG20 exibe atividade neutralizante in vivo potente contra a cepa SARS-CoV-2 original, bem como todas as variantes preocupantes conhecidas. O ADG20 tem o potencial de impactar a replicação viral e a doença subsequente através de múltiplos mecanismos de ação, incluindo o bloqueio direto da entrada viral na célula hospedeira (neutralização) e a eliminação de células hospedeiras infectadas através da atividade efetora imune inata mediada por Fc. O ADG20 é administrado por meio de uma injeção intramuscular e foi projetado para ter uma meia-vida longa, com o objetivo de fornecer proteção rápida e durável. A Adagio está avançando o ADG20 por meio de vários ensaios clínicos em uma base global.

Sobre a Adagio Therapeutics
A Adagio (Nasdaq: (ADGI) é uma empresa biofarmacêutica de estágio clínico focada na descoberta, desenvolvimento e comercialização de soluções com base em anticorpos para doenças infecciosas com potencial pandêmico. O portfólio de anticorpos da empresa foi otimizado com os recursos de engenharia de anticorpos líderes da indústria da Adimab, e foi criado para fornecer aos pacientes e médicos uma combinação de potência, amplitude, proteção durável (via extensão de meia-vida), capacidade de fabricação e acessibilidade. O portfólio de anticorpos contra SARS-CoV-2 da Adagio inclui múltiplos anticorpos amplamente neutralizantes não competitivos com epítopos de ligação distintos, liderados por ADG20. A Adagio adquiriu a capacidade de fabricação para a produção do ADG20 com fabricantes terceirizados para apoiar a conclusão de ensaios clínicos e lançamento comercial inicial, garantindo o amplo acesso para as pessoas em todo o mundo. Para mais informação, visite www.adagiotx.com.

Declarações de Previsão
Este comunicado para a imprensa contém declarações consideradas declarações de previsão de acordo com o Private Securities Litigation Reform Act of 1995. Palavras como “antecipa”, “acredita”, “espera”, “pretende”, “projeta”, e “futura”, e expressões similares são usadas para identificar declarações de previsão. As declarações de previsão incluem declarações sobre, entre outras coisas, a ocasião, progresso e resultados dos nossos estudos pré-clínicos e ensaios clínicos do ADG20, incluindo a ocasião dos nossos pedidos planejados de EUA, início e conclusão de estudos ou ensaios, e trabalhos preparatórios relacionados, o período durante o qual os resultados dos ensaios ficarão disponíveis, e nossos programas de pesquisa e desenvolvimento; nossa capacidade de obter e manter aprovações regulatórias para nossos candidatos a produtos; nossa capacidade de identificar pacientes com as doenças tratadas por nossos candidatos a produtos, e de inscrever esses pacientes nos nossos ensaios clínicos; nossas capacidades e estratégia de fabricação; e nossa capacidade de comercialização com sucesso dos nossos candidatos a produtos. Podemos não atingir os  planos, intenções ou expectativas mencionadas nas nossas declarações de previsão, e você não deve depositar confiança indevida nas nossas declarações de previsão. Essas declarações de previsão envolvem riscos e incertezas que podem fazer com que nossos resultados reais sejam substancialmente diferentes dos resultados descritos ou implícitos nas declarações de previsão, incluindo, sem limitação, os riscos descritos no título “Fatores de Risco” no Relatório Trimestral da Adagio no Formulário 10-Q do trimestre encerrado em 30 de junho de 2021 e nos futuros relatórios arquivados no SEC. Tais riscos podem ser amplificados pelos impactos da pandemia de COVID-19. As declarações de previsão contidas neste comunicado para a imprensa são válidas a partir desta data, e a Adagio não se compromete a atualizar essas informações, exceto se exigido por lei.

Contatos:

Contato com a Mídia:
Dan Budwick, 1AB
Dan@1abmedia.com

Contato com o Investidor:
Monique Allaire, THRUST Strategic Communications
monique@thrustsc.com

Adagio Therapeutics annonce de nouvelles données in vitro mettant en évidence une activité neutralisante large et puissante de l’ADG20 contre tous les variants connus du SARS-CoV-2

Les données seront présentées lors de la conférence virtuelle ISIRV-OMS 2021

WALTHAM, Massachusetts, 19 oct. 2021 (GLOBE NEWSWIRE) — Adagio Therapeutics, Inc. (Nasdaq : ADGI), une société biopharmaceutique au stade clinique axée sur la découverte, le développement et la commercialisation de solutions à base d’anticorps pour les maladies infectieuses à potentiel pandémique, a annoncé aujourd’hui de nouvelles données in vitro démontrant l’activité neutralisante conservée de son anticorps monoclonal (mAb), ADG20, contre un panel diversifié de variants du SARS-CoV-2 en circulation, y compris les variants Lambda et Mu récemment apparus. Les résultats montrent notamment que l’ADG20 exerce une puissante activité neutralisante in vitro contre tous les variants du SARS-CoV-2 préoccupants testés, y compris ceux présentant une sensibilité réduite aux produits mAb actuellement disponibles dans le cadre d’une autorisation d’utilisation en urgence (EUA, Emergency Use Authorization) ou à un stade avancé de développement. Ces données seront présentées au cours d’une séance de présentation d’affiches lors de la conférence virtuelle ISIRV-OMS 2021, qui se tiendra du 19 au 21 octobre 2021. En outre, Adagio présentera une nouvelle affiche mettant en évidence les données récemment annoncées de l’essai de phase 1 de l’entreprise portant sur l’ADG20 chez des participants en bonne santé.

« Ces nouvelles données sur les variants mettent en évidence l’efficacité potentielle de l’ADG20 contre la pandémie de COVID-19 en cours, ainsi que contre d’éventuelles épidémies futures causées par d’autres virus similaires au SARS », a déclaré Laura Walker, co-fondatrice et directrice scientifique d’Adagio. « Nous avons délibérément conçu ce mAb pour qu’il ait une activité neutralisante large et puissante, ainsi qu’une demi-vie qui étend sa fenêtre de protection potentielle — des caractéristiques essentielles qui pourraient le distinguer des autres thérapies disponibles dans le cadre d’une EUA ou en cours de développement aujourd’hui. Avec les essais mondiaux de prévention et de traitement de phase 2/3 en cours, nous sommes impatients de poursuivre notre évaluation de l’ADG20 afin d’évaluer le rôle significatif qu’il pourrait jouer dans l’arsenal des options de traitement contre la COVID-19. Administré sous forme d’injection intramusculaire unique dans les essais cliniques, l’ADG20 a été conçu pour offrir une protection allant jusqu’à un an dans le cadre de la prévention et on étudie actuellement sa possible efficacité dans le traitement des patients à haut risque et/ou en tant que complément de vaccin, y compris pour les personnes immunodéprimées. »

En plus de l’essai de phase 1 sur des participants sains, Adagio fait progresser deux essais mondiaux de phase 2/3 en cours avec l’ADG20, un essai de traitement (STAMP) et un essai de prévention (EVADE). La société prévoit de soumettre une demande d’EUA à la Food and Drug Administration des États-Unis pour l’ADG20 au cours du premier trimestre 2022.

Détails de la présentation
Titre de l’affiche : (130) Broad and Potent In Vitro Neutralization of SARS-CoV-2 Variants by ADG20, a Half-Life Extended Monoclonal Antibody in Development for the Prevention and Treatment of COVID-19 (Neutralisation large et puissante in vitro des variants du SARS-CoV-2 par l’ADG20, un anticorps monoclonal à demi-vie prolongée en cours de développement pour la prévention et le traitement du COVID-19)

Titre de l’affiche  :(131) Evaluating the Safety, Tolerability, and Pharmacokinetics of ADG20, a Half-Life–Extended Monoclonal Antibody (mAb) in Development for the Prevention and Treatment of COVID-19: a Preliminary Analysis of a Randomized Phase 1 Study (Évaluation de l’innocuité, de la tolérabilité et de la pharmacocinétique de l’ADG20, un anticorps monoclonal (mAb) à demi-vie prolongée en cours de développement pour la prévention et le traitement de la COVID-19 : une analyse préliminaire d’une étude randomisée de phase 1)

À propos de l’ADG20
L’ADG20, un anticorps monoclonal ciblant la protéine spike du SARS-CoV-2 et des coronavirus connexes, est en cours de développement aux fins de la prévention et du traitement de la COVID-19, la maladie provoquée par le SARS-CoV-2. L’ADG20 a été conçu et élaboré en vue d’offrir de puissantes et vastes capacités de neutralisation du SARS-CoV-2 et des autres sarbecovirus du clade 1 permettant de cibler un épitope bien conservé dans le domaine de fixation du récepteur. L’ADG20 exerce une puissante activité neutralisante in vivo contre la souche originale du SARS-CoV-2 et tous ses variants préoccupants connus. L’ADG20 pourrait avoir un impact sur la réplication virale et la maladie subséquente grâce à de multiples mécanismes d’action, notamment le blocage direct de l’entrée virale dans la cellule hôte (neutralisation) et l’élimination des cellules hôtes infectées par l’activité effectrice immunitaire innée médiée par Fc. L’ADG20 est administré par une seule injection intramusculaire et a été conçu pour avoir une longue demi-vie, dans le but de fournir une protection à la fois rapide et durable. Adagio fait progresser l’ADG20 grâce à de multiples essais cliniques à l’échelle mondiale.

À propos d’Adagio Therapeutics
Adagio (Nasdaq : ADGI) est une société biopharmaceutique au stade clinique axée sur la découverte, le développement et la commercialisation de solutions à base d’anticorps pour les maladies infectieuses présentant un potentiel pandémique. Le portefeuille d’anticorps de la société a été optimisé grâce aux capacités de pointe d’Adimab en matière d’ingénierie d’anticorps et est conçu pour fournir aux patients et aux cliniciens une combinaison inégalée de puissance, d’ampleur, de protection durable (grâce à l’extension de la demi-vie), de faisabilité de fabrication et de prix abordable. Le portefeuille d’anticorps anti-SARS-CoV-2 d’Adagio comprend plusieurs anticorps fortement neutralisants non concurrents dotés d’épitopes de liaison distincts, dirigés par l’ADG20. Adagio a conclu avec des sous-traitants tiers un contrat portant sur des capacités de fabrication pour la production de l’ADG20 afin de soutenir l’achèvement des essais cliniques et le lancement commercial initial, garantissant ainsi une large accessibilité aux populations du monde entier. Pour plus d’informations, rendez-vous sur notre site www.adagiotx.com.

Énoncés prospectifs
Le présent communiqué de presse contient des énoncés prospectifs au sens de la loi Private Securities Litigation Reform (Réforme sur la résolution des litiges portant sur des titres privés) de 1995. Des mots tels que « anticipe », « croit », « s’attend à », « l’intention », « des projets » et « à l’avenir » ou des expressions similaires sont destinés à identifier des énoncés prospectifs. Les énoncés prospectifs comprennent des énoncés concernant, entre autres, le calendrier, les progrès et les résultats de nos études précliniques et essais cliniques sur l’ADG20, y compris le calendrier de notre demande d’EUA prévue, le lancement et l’achèvement d’études ou d’essais et de travaux préparatoires connexes, la période durant laquelle les résultats des essais seront disponibles et nos programmes de recherche et développement ; notre capacité à obtenir et conserver des approbations réglementaires pour nos produits candidats ; notre capacité à identifier les patients atteints des maladies traitées par nos produits candidats et à recruter ces patients dans nos essais cliniques ; nos capacités et notre stratégie de fabrication ; et notre capacité à commercialiser avec succès nos produits candidats. Nous pourrions ne pas réellement atteindre les plans, intentions ou attentes divulgués dans nos énoncés prospectifs et vous ne devez pas vous fier indûment à nos énoncés prospectifs. Ces énoncés prospectifs impliquent des risques et des incertitudes qui pourraient faire en sorte que nos résultats réels diffèrent sensiblement des résultats décrits ou sous-entendus par les énoncés prospectifs, y compris, sans s’y limiter, les risques décrits sous la rubrique « Risk Factors » (Facteurs de risque) dans le rapport trimestriel d’Adagio sur le formulaire 10-Q pour le trimestre clos le 30 juin 2021 et dans les futurs rapports qu’Adagio déposera auprès de la SEC. De tels risques peuvent être amplifiés par les impacts de la pandémie de COVID-19. Les énoncés prospectifs contenus dans le présent communiqué de presse sont formulés à cette date, et Adagio décline toute obligation de mettre à jour ces informations sauf si la loi en vigueur l’exige.

Contacts :

Contact auprès des médias :
Dan Budwick, 1AB
Dan@1abmedia.com

Contact auprès des investisseurs :
Monique Allaire, THRUST Strategic Communications
monique@thrustsc.com

Bill & Melinda Gates Foundation Commits up to $120 Million to Accelerate Access to COVID-19 Drug for Lower-Income Countries, Calls on Other Donors to Mobilize Resources

Financial commitment aims to secure dedicated, low-cost supply of molnupiravir, if the drug is authorized by regulators; builds on long-term efforts to increase access to tests, treatments, vaccines

SEATTLE, Oct. 20, 2021 /PRNewswire/ — The Bill & Melinda Gates Foundation announced today a commitment of up to $120 million to accelerate access to the investigational antiviral drug molnupiravir for lower-income countries as part of its COVID-19 response effort. The funding will be allocated based on consultations with partners, and will support the range of activities required to develop and manufacture generic versions of the drug, which is being developed by Merck & Co in collaboration with Ridgeback Biotherapeutics.

This commitment builds on the foundation’s ongoing efforts, including $1.9 billion in funding, since the start of the pandemic to increase access to COVID-19 vaccines, treatments, and tests by supporting R&D, regulatory work, at-risk manufacturing, and product delivery.

“To end this pandemic, we need to ensure that everyone, no matter where they live in the world, has access to life-saving health products. The unjust reality, however, is that low-income countries have had to wait for everything from personal protective equipment to vaccines. That is unacceptable,” said Melinda French Gates, co-chair of the Gates Foundation. “Today’s commitment will ensure that more people in more countries get access to the promising drug molnupiravir, but it’s not the end of the story—we need other donors, including foundations and governments, to act.”

Initial data reported by Merck suggest that molnupiravir, a broad-spectrum antiviral, can cut the risk of serious disease and death due to COVID-19 by half. Molnupiravir would be the first oral outpatient drug authorized for use in treating COVID-19 patients with mild and moderate disease—a critical breakthrough to prevent hospitalizations and save lives in combination with increased vaccination coverage and existing treatments for severely and critically ill patients. The decision on whether to authorize the drug for use sits with regulatory agencies, including the World Health Organization (WHO) and national governments.

“Africa CDC and the Africa Union have been tracking the exciting developments on the antiviral, molnupiravir,” said John Nkengasong, director of the Africa Centers for Disease Control and Prevention. “In order to make sure that Africa is not left behind, we have been working with the Bill & Melinda Gates Foundation colleagues on various mechanisms they can facilitate, once all of the regulatory processes are completed and the drug is officially made available to the world.”

This commitment leverages the resources of the foundation’s Strategic Investment Fund, which uses a suite of financial tools—including loans and volume guarantees—to address market failures and incentivize private enterprises to develop affordable and accessible health products. The foundation’s previous work to lower costs and increase access to life-saving drugs includes dolutegravir, an HIV drug. In 2017, the foundation established a volume guarantee with two generic suppliers that has brought therapies containing the drug to more than 18 million people in lower-income countries, in coordination with the U.S. President’s Emergency Plan for AIDS Relief (PEPFAR) and the Global Fund to Fight AIDS, Tuberculosis and Malaria.

Strive Masiyiwa, African Union special envoy on COVID-19 response, said, “We applaud the foundation for its commitment and look forward to continuing our collaboration to ensure this potentially lifesaving treatment, upon regulatory approval, is accessible to as many Africans as possible. This would be a step forward in balancing the inequities seen to date in availability of innovations during the pandemic.”

The foundation has already provided expertise and funding to help strengthen generics manufacturers, including $1.3 million to Medicines for All Institute (M4ALL) and the University of Manchester to develop low-cost manufacturing processes that dramatically reduce the cost of raw materials and increase product yields. Several generics manufacturers are investigating these improvements already as they plan to scale up production following regulatory authorization. The foundation has also provided $2.4 million in grants to expedite generic company readiness to apply for WHO prequalification and start manufacturing when prequalification is granted.

“Merck has taken important steps to make this drug available as a COVID-19 therapy, including negotiating licenses with generics manufacturers to increase supply. We are pleased to work alongside these efforts to ensure affordability and availability in lower-income countries,” said Bill Gates, co-chair of the Gates Foundation. “Making life-saving drugs like these available to everyone who needs them is what is necessary to end the acute phase of the pandemic, and open pathways to recovery.”

The goal is to significantly reduce the time it takes for a new drug to reach low-income countries after it becomes available in high-income markets. The standard gap in rolling out global health products can be 12 months or more.

“We have a unique set of resources and expertise that we dedicate to ensuring that everyone, everywhere has access to life-saving health interventions,” said Mark Suzman, chief executive officer of the Gates Foundation. “This is what the foundation does best. We will work with companies, procurement agencies, and donors to make molnupiravir available to low-income countries. Our funding is part of what’s needed to ensure equitable supply. We call on other donors and partners to help mobilize the multiples of additional resources required.”

Since the start of the pandemic, the foundation has worked closely with a range of partners on R&D and delivery of COVID-19 tools. These partners include philanthropic and government donors that are part of the COVID-19 Therapeutics Accelerator and global organizations in the therapeutics pillar of the access to COVID-19 Tools Accelerator (ACT-A) partnership, including Unitaid, UNICEF, WHO, the Global Fund, Wellcome, and the Africa Medical Supplies Platform. The foundation will continue to work with multilateral organizations, nongovernmental organizations, governments, and other partners to ensure that clinical, regulatory, and delivery pathways are ready once molnupiravir and its generic versions become available.

About the Bill & Melinda Gates Foundation
Guided by the belief that every life has equal value, the Bill & Melinda Gates Foundation works to help all people lead healthy, productive lives. In developing countries, it focuses on improving people’s health and giving them the chance to lift themselves out of hunger and extreme poverty. In the United States, it seeks to ensure that all people—especially those with the fewest resources—have access to the opportunities they need to succeed in school and life. Based in Seattle, Washington, the foundation is led by CEO Mark Suzman, under the direction of Bill Gates and Melinda French Gates.

Media contact: media@gatesfoundation.org

SADC Governments Crafting Cyber Laws That Infringe on Citizens, says Professor

A prominent professor studying communication in Namibia says member countries in the 16-nation Southern African Development Community, or SADC, have enacted and drafted cybersecurity laws which infringe on citizens’ freedom of expression. Zimbabwe is one of the southern African nations that critics say has drafted strict cybersecurity laws in the region — awaiting President Emmerson Mnangagwa’s signature.

A professor in Namibia said most cybersecurity laws in the region infringe on the right to privacy and freedom of expression and are in need of revision.

Admire Mare is a professor of communication, journalism and media technology at Namibia University of Science. This week, he published a report examining how basic freedoms should be at the core of policies lawmakers should consider when drafting laws.

“Human rights should be at the center of policy making and drafting of legislation. If you miss that out you may actually end up infringing, curtailing the exercise of some of the basic rights that human beings must be able to [enjoy],” he said.

The report titled “Cybersecurity and Cybercrime Laws in the SADC Region: Implications on Human Rights,” looks at several countries in the region. However, Mare singles out South Africa as one of the few 16-nation member countries with laws taking citizens’ freedoms into account.

Tabani Moyo is the director of the Harare-based Media Institute of Southern Africa, or MISA, an organization with SADC member representatives, where the report was launched. He called on President Mnangagwa to rethink Zimbabwe’s Cyber Security and Data Protection Bill and reverse course from signing the bill into law. The bill was recently passed by parliament and critics say it punishes social media users for minor infractions.

Moyo said the bill, if signed as is, only empowers few people.

“It fails to provide protection for a whistleblower in a comprehensive manner. Secondly, it provides the security forces the power to snoop into our communication through the Cyber Security Center [Zimbabwe’s cybersecurity agency]. Thirdly, it is just impossible to define interference with personal data without [providing] legal oversight from the judiciary,” he said.

Moyo said the bill creates loopholes for authorities to abuse citizens similar to what is happening in Lesotho, Tanzania and Zambia.

Human rights advocates say authorities in these countries have routinely used laws to arrest opposition members and curtail their activities. But the bill has some supporters.

Lawyer and information and communications technology expert, Jacob Mutevedzi, praised Zimbabwe’s parliament for passing what he calls a “progressive and commendable cyber statute.”

“Prior to this law [bill awaiting signature to be implemented] the legal framework for cyber security and data protection in Zimbabwe was incoherent and half baked. The country lacked a comprehensive legal framework for the regulation of cybersecurity and data protection. The consolidation of cyber related offences and regulation of data protection under the current statute within a single framework is a welcome development which accords with regional practices,” said Mutevedzi.

Professor Mare, however, said it is also the responsibility of rights organizations like MISA to take action against the cyberlaws endangering journalists and citizens’ rights.

“Strategic litigation — we have seen in different countries — can be an opportunity that can be harnessed. Make use of public interest lawyers and to test the constitutionality of some of these proposed and enacted laws,” said Mare.

Zimbabwe’s government has for long insisted that it needs a tight cyberlaw to deal with what it calls “falsehoods” peddled especially on social media.

Source: Voice of America

New Airstrikes Target Capital of Ethiopia’s Tigray Region

Ethiopian forces have carried out another airstrike on the capital city of the northern Tigray region Wednesday, two days after an airstrike killed three children there.

United Nations spokesman Farhan Haq told reporters Tuesday that one other person was killed in the airstrike on the outskirts of Mekelle. Haq said nine people were reportedly injured in a second airstrike in Mekelle later that day that also damaged a number of houses and a nearby hotel.

The spokesman said the U.N.’s colleagues “are alarmed at the intensification of the conflict and once again remind all parties to the conflict of their obligations under international humanitarian law to protect civilians and civilian infrastructure.”

The Ethiopian government initially denied launching Monday’s attacks, but the state-run Ethiopian Press Agency later acknowledged the airstrikes and said they targeted communications infrastructure.

“Action [was taken] against media and equipment used by the TPLF [Tigray People’s Liberation Front] terrorists in Mekelle,” the press statement said. The TPLF is a former member of the coalition that ruled Ethiopia for more than 30 years. In May, Ethiopia designated the group a terrorist organization.

Getachew Reda, a TPLF spokesperson, accused Ethiopia’s prime minister, Abiy Ahmed, of being unwilling to end the conflict. “He has never been for peace, only the appropriate use of sticks can prod him into considering such a path. The #AirStrikeonCivilians in #Mekelle is proof positive that he will do everything to terrorize our people, especially when his forces are losing on the battlefield,” he said in a Twitter post Tuesday. “If people had illusions he could keep his promise to resolve the conflict peacefully, yesterday’s attack should make it clear that only sticks are effective.”

The Ethiopian federal government has been engaged in an armed conflict with fighters from the northern Tigray region for nearly a year.

Mekelle has not seen large-scale fighting since June, when Ethiopian forces withdrew from the area and Tigray forces retook control of most of the region. Following that, the conflict continued to spill into the neighboring regions of Amhara and Afar.

Last week, Tigray forces said the Ethiopian military had launched a ground offensive to push them out of Amhara.

Source: Voice of America