Clinical development partner

Initiation of the First-in-Human trial with Dyadic’s SARS-CoV-2-RBD vaccine candidate DYAI-100

26

Jan

2023

CR2O is happy to announce that the First-in-Human trial with Dyadic’s SARS-CoV-2-RBD vaccine candidate DYAI-100 has started in South Africa.

Dyadic International Inc. is a global biotechnology company focused on further improving, applying and deploying its proprietary C1-cell protein production platform to accelerate development, lower production costs and improve the performance of biologic vaccines and drugs at flexible commercial scales. Dyadic has entered into a master services agreement with CR2O, as full-service global contract research organization specializing in vaccinology, to manage preclinical and clinical development of Dyadic’s SARS-CoV-2–RBD vaccine candidate DYAI-100.

In July 2022, CR2O (on behalf of Dyadic) submitted a Clinical Trial Application (CTA) to the South African Health Products Regulatory Authority (SAHPRA) and the Witwatersrand Human Research Ethics Committee (WHREC) in order to gain approval to initiate a Phase I study with DYAI-100, a C1-SARS-CoV-2 recombinant protein RBD vaccine and clearance to start the trial was provided in October 2022.

The Phase I randomized, double blind, placebo-controlled trial is designed to demonstrate clinical safety and preliminary efficacy of DYAI-100.

Following the regulatory approval from the South African Health Products Regulatory Authority (SAHPRA) and the Witwatersrand Human Research Ethics Committee (WHREC), site preparations and recruitment was commenced and the first dosing for subjects began during the week of January 9th, 2023.

The Chief Scientific Officer of CR2O, Prof. Albert Osterhaus, applauds the collaborative efforts of Dyadic and CR2O. These have led to the approval and execution of this first in human Phase I trial with a candidate COVID-19 booster vaccine, produced with the novel C1-cell protein production platform. The use of this platform may well pave the way for faster, cheaper and easier production of vaccines and other biologicals to combat emerging viruses.

For Dyadic’s original press release, please refer to GlobeNewswire.

Curious to learn more about CR2O’s full-service global CRO activities, or experience with vaccine trials?
Please, contact Ellemieke von Mauw:

Ellemieke von Mauw
Director Clinical Programs | Business Development
CR2O B.V.

T +31 (0)85 071 74 65 | M +31 (0)6 57 76 61 45 | E Ellemieke.vonmauw@cr2o.nl

CR2O to manage First-in-Human trial with Dyadic’s SARS-CoV-2-S-RBD vaccine candidate DYAI-100

21

May

2023

CR2O is proud to announce today it will manage and further support the clinical and preclinical development of DYAI-100, Dyadic’s C1 produced SARS-CoV-2-S-RBD vaccine candidate.

The first-in-human trial with DYAI-100 is expected to begin in H2 2021. 

Dyadic International Inc., a global biotechnology company focused on further improving, applying and deploying its proprietary C1-cell protein production platform to accelerate development, lower production costs and improve the performance of biologic vaccines and drugs at flexible commercial scales, announced on March 18 2021 that the company’s initial C1 produced SARS-CoV-2-S-RBD vaccine candidate, DYAI-100,  is moving towards an anticipated safety and preliminary efficacy first-in-human Phase I clinical trial. Dyadic has entered into a master services agreement with CR2O, as full-service global contract research organization specializing in vaccinology, to manage preclinical and clinical development of DYAI-100.

CR2O’s Chief Scientific Officer, Prof. Dr. Albert Osterhaus commented, “In response to the COVID-19 pandemic, pharmaceutical companies have developed vaccines within the unprecedented period of less than one year. To this end, and in close collaboration with strategic partners, they have implemented state-of-the-art technologies including the use of mRNA, viral vectors, and novel adjuvants. To effectively combat the COVID-19 pandemic worldwide, second generation variants of concern vaccines, produced at low cost and in large scale, are now urgently needed. The collaboration with Dyadic to use their highly-productive fungal C1-cell protein manufacturing system for this purpose appears to be a logical and promising way forward.”

CR2O’s CEO, Hadil Es-Sbai, added: “We are honoured to partner with Dyadic and its strategic partners in developing an affordable, scalable, protective and safe vaccine to combat this disease that continues to impact our everyday life”

For Dyadic’s original press release, please refer to Yahoo Finance.

Curious to learn more about CR2O’s full-service global CRO activities, or experience with vaccine trials?
Please, contact Ellemieke von Mauw:

Ellemieke von Mauw
Director Clinical Programs | Business Development
CR2O B.V.

T    +31 (0)85 071 74 65    |    M     +31 (0)6 57 76 61 45 E    |    Ellemieke.vonmauw@cr2o.nl

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H2020 awards contract to develop a monoclonal antibody against COVID-19

09

Apr

2020

The EU Research and Innovation programme HORIZON 2020 has awarded a contract worth up to 3 million euro’s to a European consortium led by ErasmusMC in collaboration with Harbour Antibodies BV to develop a monoclonal antibody against SARS-CoV 2.

This project “MANCO” aims at the development of contributing to the rapid international public health preparedness and response against the novel coronavirus SARS CoV 2 that emerged in China at the end of 2019. Coronavirus disease (COVID-19) is an infectious disease caused by this newly discovered coronavirus SARS CoV 2.

Most people infected with the SARS CoV 2 virus will experience mild to moderate respiratory illness and recover without requiring special treatment.  Older people, and those with underlying medical problems like cardiovascular disease, diabetes, chronic respiratory disease, and cancer are more likely to develop serious illness.

At this time, there are no specific vaccines or treatments for COVID-19.

Lessons learned and intervention efforts against SARS coronavirus (CoV), MERS-CoV and other emerging viruses provide invaluable information to accelerate the coordinated response against SARS-CoV 2 and the rapid development and manufacture of new diagnostic, prophylactic and therapeutic intervention strategies for COVID 19. A much-promising approach to both patient management of emerging viral infections and to better preparedness and response to emerging epidemics is the use of monoclonal antibodies. The consortium aims at contributing to the rapid international response against COVID 19, through preclinical and clinical evaluation of monoclonal antibodies against SARS-CoV 2.

In this consortium 8 partners have joined to develop a monoclonal antibody against Sars-CoV 2. As one of the partners CR2O BV will coordinate the phase I clinical trial and assume the role of the sponsor of the clinical trial.