Vein graft failure

Pluri’s PLX-R18 Increases Blood Cell Counts and Reduces Need for Transfusions in a Phase I Study: Results Published in Nature Bone Marrow Transplantation

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수요일, 8월 16, 2023

As described in the article, in a successful Phase I first-in-human study which achieved its primary endpoint, patients with incomplete hematopoietic recovery post-hematopoietic cell transplantation (HCT) were treated with escalating doses of Pluri’s cell therapy, PLX-R18.

Key Points: 
  • As described in the article, in a successful Phase I first-in-human study which achieved its primary endpoint, patients with incomplete hematopoietic recovery post-hematopoietic cell transplantation (HCT) were treated with escalating doses of Pluri’s cell therapy, PLX-R18.
  • Low levels of blood cells (cytopenia) post-HCT can persist despite adequate engraftment of donor cells.
  • Pluri’s PLX-R18 cells secrete a large array of hematopoietic factors which promote regeneration, maturation, and differentiation of hematopoietic cells and stimulate their migration to peripheral blood.
  • As a groundbreaking, first-in-class solution, PLX-R18’s capacity to augment hematopoietic system recovery and effectively manage diverse cytopenia holds immense promise.”

FDA Approves Cell Therapy for Patients with Blood Cancers to Reduce Risk of Infection Following Stem Cell Transplantation

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월요일, 4월 17, 2023

"Today's approval is an important advance in cell therapy treatment in patients with blood cancers," said Peter Marks, M.D., Ph.D., director of the FDA's Center for Biologics Evaluation and Research.

Key Points: 
  • "Today's approval is an important advance in cell therapy treatment in patients with blood cancers," said Peter Marks, M.D., Ph.D., director of the FDA's Center for Biologics Evaluation and Research.
  • "Hastening the return of the body's white blood cells can reduce the possibility of serious or overwhelming infection associated with stem cell transplantation.
  • Blood cancers are a form of cancer caused by uncontrolled growth of cells in the blood, disrupting the ability of blood cells to perform their normal functions.
  • Blood cancers can be fatal, with varying survival rates based on multiple factors including the specific type of blood cancer diagnosed.

Eurofins Viracor and Cornell University Sign Exclusive Licensing Agreement to Expand Access to Ground-Breaking Technologies for Assessing Organ and Tissue Damage in Transplant and COVID-19 Patients

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목요일, 3월 17, 2022

LEE'S SUMMIT, Mo., March 17, 2022 /PRNewswire/ -- Eurofins Viracor, LLC, a leader in testing for infectious disease, immunology, and allergy, announced today that it has entered into an exclusive license agreement with Cornell University to commercialize several ground-breaking and novel assays aimed at transforming the clinical management of COVID-19 and transplant patients impacted from tissue damage and infections.

Key Points: 
  • Surgical biopsy is critical in tracking damage of COVID-19 in the body, but the procedure can be painful and costly to the patient.
  • The test uses circulating cell-free DNA (cfDNA) to gauge the damage that COVID-19 inflicts on cells, tissues and organs.
  • The agreement between Eurofins Viracor and Cornell University will expand access to an innovative blood-based cfDNA methylation sequencing assay for early detection or prediction of major complications related to allogeneic HCT, thus improving the care of stem cell transplant patients.
  • Shares in Eurofins Scientific are listed on the Euronext Paris Stock Exchange (ISIN FR0000038259, Reuters EUFI.PA, Bloomberg ERF FP).

Marizyme Announces Allowance of Patent Application for Flagship Product DuraGraft by United States Patent and Trademark Office

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수요일, 1월 5, 2022

DuraGraft, the only product approved for graft protection and preservation during bypass and other vascular surgeries, is currently approved and marketed in Europe and several other leading global healthcare markets.

Key Points: 
  • DuraGraft, the only product approved for graft protection and preservation during bypass and other vascular surgeries, is currently approved and marketed in Europe and several other leading global healthcare markets.
  • Marizyme is actively seeking United States FDA approval for DuraGraft.
  • Allowance of this DuraGraft patent application in the United States represents a significant milestone for us, stated David Barthel, Marizymes CEO, and protects our commercial opportunities for DuraGraft in the US.
  • DuraGraft enhances coronary artery bypass grafting (CABG) surgical outcomes by significantly reducing major adverse cardiac events such as repeat revascularization and myocardial infarction.

Marizyme Announces the Closing of My Health Logic Acquisition Along With Initial Financing

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목요일, 12월 23, 2021

JUPITER, Fla., Dec. 23, 2021 (GLOBE NEWSWIRE) -- via NewMediaWire -- Marizyme Inc. (Marizyme or the Company) (OTCQB:MRZM), is pleased to announce the closing of its acquisition of My Health Logic Inc., a subsidiary of Health Logic Interactive Inc. (TSXV:CHIP.H), along with a concurrent financing.

Key Points: 
  • JUPITER, Fla., Dec. 23, 2021 (GLOBE NEWSWIRE) -- via NewMediaWire -- Marizyme Inc. (Marizyme or the Company) (OTCQB:MRZM), is pleased to announce the closing of its acquisition of My Health Logic Inc., a subsidiary of Health Logic Interactive Inc. (TSXV:CHIP.H), along with a concurrent financing.
  • My Health Logics lab-on-chip technology platform and patient-centric digital point-of-care device, MATLOC 1, further strengthens Marizymes life science technology product pipeline.
  • Mr. Kovalyov is a founding member of the My Health Logic team and is a CPA with cross border transaction experience.
  • My Health Logic is developing and commercializing consumer focused handheld point-of-care diagnostic devices that connect to patient's smartphones and digital continued care platforms.

Marizyme Inc. Announces Results of GOAL Study Presented at 7th Annual International Coronary Congress

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금요일, 12월 3, 2021

The GOAL Study is an independent investigator observational clinical study to assess the role of vascular graft /storage solutions on myocardial protection during coronary artery bypass grafting (CABG) surgeries.

Key Points: 
  • The GOAL Study is an independent investigator observational clinical study to assess the role of vascular graft /storage solutions on myocardial protection during coronary artery bypass grafting (CABG) surgeries.
  • The study was comprised of two cohorts, each cohort consisting of 83 propensity-matched patients undergoing on-pump CABG surgery.
  • The propensity score-based study we presented today validates and confirms our initial findings across a larger patient base.
  • Building on this, the results from the GOAL study are very exciting.

Marizyme Announces Expansion of Patent Portfolio Into Several Key Territories

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금요일, 12월 3, 2021

Marizyme also announced today that it has retained the services of Dentons US LLP , the worlds largest law firm with more than 600 international patent lawyers and professionals in more than 80 countries, to manage its global patent portfolio.

Key Points: 
  • Marizyme also announced today that it has retained the services of Dentons US LLP , the worlds largest law firm with more than 600 international patent lawyers and professionals in more than 80 countries, to manage its global patent portfolio.
  • Patent applications covering the companys flagship commercial product, DuraGraft,have been allowed in Brazil, China and Malaysia.
  • Additionally, Malaysia represents a key territory in Asia Pacific in which we already have a significant customer base.
  • Krillase is not approved for use in the U.S. For more information about Marizyme, visitwww.marizyme.com

InsightRX's Precision Medicine Technology to Help Improve Care for Patients Receiving Stem Cell Transplants

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월요일, 11월 22, 2021

The InsightRX Nova platform helps to select patient-specific doses of the chemotherapy drugs busulfan and fludarabine, as well as the immunosuppressant anti-thymocyte globulin (ATG), for adult and pediatric patients receiving stem cell transplants.

Key Points: 
  • The InsightRX Nova platform helps to select patient-specific doses of the chemotherapy drugs busulfan and fludarabine, as well as the immunosuppressant anti-thymocyte globulin (ATG), for adult and pediatric patients receiving stem cell transplants.
  • Stem cell transplants typically are preceded by a chemotherapeutic conditioning regimen that destroys cancer cells and suppresses a patient's immune response to the donor cells.
  • The five-year cumulative mortality rate for leukemia patients receiving a stem cell transplant is about 50%, with relapse, infection, and GvHD as the leading causes of death.
  • InsightRX is a healthcare technology company that has developed a cloud-based platform for precision medicine and clinical analytics designed to individualize treatment at the point of care.

Marizyme is Pleased to Announce the Appointment of David Barthel as CEO

Retrieved on: 
화요일, 11월 16, 2021

JUPITER, Fla., Nov. 16, 2021 (GLOBE NEWSWIRE) -- via NewMediaWire -- Marizyme Inc. (Marizyme or the Company) (OTCQB:MRZM), is pleased to announce the hiring of Mr. David Barthel as the Chief Executive Officer for Marizyme.

Key Points: 
  • JUPITER, Fla., Nov. 16, 2021 (GLOBE NEWSWIRE) -- via NewMediaWire -- Marizyme Inc. (Marizyme or the Company) (OTCQB:MRZM), is pleased to announce the hiring of Mr. David Barthel as the Chief Executive Officer for Marizyme.
  • Mr. Barthel founded The SmartPill Corp. and led the company as CEO & President until its acquisition by medical device giant, Medtronic.
  • Mr. Barthel led his team through multiple clinical trials, manufacturing, FDA approval, commercialization and successful insurance reimbursement.
  • After the acquisition by Medtronic, Mr. Barthel joined the company as Area Vice President, GIH Southeast Division.

Health Logic Interactive Signs Non-Binding Letter of Intent With US Medical Device Company to Sell Wholly Owned Operating Subsidiary

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월요일, 8월 9, 2021

CALGARY,AB, Aug. 9, 2021 /PRNewswire/ -Health Logic Interactive Inc. ("Health Logic" or the "Company") (TSXV: CHIP.H) (OTCPK: CHYPF) is pleased to announce it has signed, on August 1, 2021, a non-binding letter of intent to sell its wholly owned operating subsidiary,My Health LogicInc.

Key Points: 
  • CALGARY,AB, Aug. 9, 2021 /PRNewswire/ -Health Logic Interactive Inc. ("Health Logic" or the "Company") (TSXV: CHIP.H) (OTCPK: CHYPF) is pleased to announce it has signed, on August 1, 2021, a non-binding letter of intent to sell its wholly owned operating subsidiary,My Health LogicInc.
  • ("My Health Logic") to Marizyme, Inc. ("Marizyme"), a Nevada medical device company publicly traded on the OTCQB (the "Transaction").
  • The proposed terms, which are subject to change as diligence and negotiations progress, include:
    The Company receiving 4,600,000 shares of Marizyme as consideration for the Health Logic asset.
  • Health Logic Interactive, through its wholly owned operating subsidiary My Health Logic, is developing and commercializing consumer focused handheld point-of-care diagnostic devices that connect to patient's smartphones and digital continued care platforms.