| Name | Title | Contact Details |
|---|
Since its beginning, Feldan has valued internal research with the aim of innovating, changing standards of care and redefining quality of life. With the recent development of the Feldan Shuttle, this approach is starting to show its promises. Feldan`s mission is to develop regenerative medicine therapeutic applications based on Feldan`s proprietary technology.
Criada em 1977, são mais de quatro décadas de uma história construída com qualidade, acessibilidade e inovação, sempre com o foco no bem-estar da população brasileira. Sobre a Cimed: Somos uma das maiores farmacêuticas do país. Com mais de 40 anos de história, uma das poucas empresas do setor que permanece totalmente brasileira e independente até hoje. São mais de 600 produtos no catálogo e uma distribuição nacional para mais de 60 mil pontos de vendas. Além disso, a Cimed é líder em todos os setores em que atua. Temos nosso complexo fabril em Pouso Alegre (MG), o centro de distribuição central e a gráfica em São Sebastião da Bela Vista (MG), além de contar com 25 centros de distribuição espalhados pelo país. Com sede administrativa em São Paulo, são cerca de 5 mil colaboradores em todo Brasil. Somos, também, apoiadores do esporte nacional, patrocinando a Confederação Brasileira de Futebol. Projeto +: Mais de 280 mil m², esse é o tamanho do terreno da nova fábrica de sólidos orais da Cimed em Pouso Alegre, no Sul de Minas Gerais, a ser finalizada até 2022. A nova unidade terá aproximadamente 44 mil m² de área construída, fazendo com que a capacidade produtiva da área de sólidos passe de 28 milhões para 40 milhões comprimidos por mês, podendo chegar a 60 milhões. Pesquisa e Desenvolvimento: A Cimed é uma das poucas empresas do setor a ter o seu próprio centro de bioequivalência e a única a realizar todas as etapas de estudo necessárias para o registro de medicamentos genéricos e similares (clínica, analítica e estatística). Tudo isso é feito no Instituto Claudia Marques de Pesquisa e Desenvolvimento (ICM P&D), criado em 2004. Nossos números - Mais de 5 mil colaboradores - Mais de 60 mil pontos de venda - Presentes em mais de 90% das farmácias brasileiras - Cerca de 600 produtos no portfólio
Sierra Oncology is a clinical stage drug development company advancing targeted therapeutics for the treatment of patients with unmet medical needs in hematology and oncology. Our lead drug candidate, momelotinib, is a potent, selective and orally-bioavailable JAK1, JAK2 & ACVR1 inhibitor with a differentiated therapeutic profile in myelofibrosis encompassing a range of meaningful anemia benefits, including eliminating or reducing the need for frequent blood transfusions, as well as achieving substantive spleen and constitutional symptom control. We are also advancing SRA737 and SRA141. SRA737, is a potent, highly selective, orally bioavailable small molecule inhibitor of Checkpoint kinase 1 (Chk1). We are pursuing an innovative development plan for SRA737, which is currently being evaluated in two Phase 1/2 clinical trials in patients with advanced cancer. SRA737-01 is intended to evaluate SRA737`s potential to induce synthetic lethality as monotherapy, while SRA737-02 is intended to evaluate the combination of SRA737 potentiated by subtherapeutic, low dose gemcitabine. Concurrently, we are conducting preclinical research evaluating SRA737 in combination with other DDR-targeted agents, including PARP inhibitors, as well as with immuno-oncology therapeutics, that may guide a potential next wave of clinical development for our asset, possibly further broadening its therapeutic utility. SRA141, a potent, selective, orally bioavailable small molecule inhibitor of cell division cycle 7 kinase (Cdc7). Cdc7 is a key regulator of DNA replication and is involved in the DDR network, making it a compelling emerging target for potential treatment across a broad range of tumor types. An Investigational New Drug Application (IND) submission to the U.S. Food and Drug Administration (FDA) is being prepared in order to commence clinical trials with this drug candidate.
Vor Biopharma is pioneering engineered hematopoietic stem cells (eHSCs) to dramatically change the treatment paradigm for hematological cancers. Vor`s eHSCs are designed to generate healthy, fully functional cells with specific advantageous modifications, for example to protect the blood and bone marrow from the toxic effects of antigen-targeted therapies, protecting healthy cells from depletion but leaving tumor cells vulnerable. Vor`s platform could potentially be used to change the treatment paradigm of both hematopoietic stem cell transplants and antigen-targeted therapies such as antibody drug conjugates, bispecific antibodies and CAR-T cell treatments. A proof-of-concept study for Vor`s lead program has been published in Proceedings of the National Academy of Sciences. Vor is based in Cambridge, Mass. and has a broad intellectual property base including in-licenses from Columbia University, where foundational work was conducted by inventor and Vor Scientific Board Chair Siddhartha Mukherjee, MD, DPhil. Vor was founded by Dr. Mukherjee and PureTech Health and is supported by leading investors including 5AM Ventures and RA Capital Management, Johnson & Johnson Innovation – JJDC, Inc. (JJDC), Novartis Institutes for BioMedical Research and Osage University Partners.