ZEUS Scientific Acquires Synthetic Peptides from Sheba Medical Center’s Tech Transfer Co.

Could Hold the Clue to Creating Better Treatments for Rheumatoid Arthritis

ZEUS Scientific has obtained exclusive, worldwide rights to the use of these synthetic peptides as targets of disease-specific autoantibodies in Rheumatoid Arthritis (RA) from Sheba Medical Center’s, Tel Hashomer Medical Research, Infrastructure and Services Ltd. (Tel Hashomer Ltd.) the hospital’s Technology Transfer Company (TTO).

The inventors, Professor Howard Amital, Professor Yehuda Shoenfeld and Dr. Smadar Gertel from Sheba Medical Center, created synthetic peptides, including peptides comprising a plurality of epitopes, with each epitope being derived from a different protein, and peptides comprising a plurality of citrullinated residues (Patented by Sheba Medical Center (US Patent 9,975,944 B2).

ZEUS Scientific intends to utilize these innovative multi-epitope citrullinated peptides for the development of a new generation of immunoassays designed to measure autoantibodies as an aid in the diagnosis of Rheumatoid Arthritis.

This invention marks a new era in the evolution of citrullinated peptides.

“We are pleased to have executed this licensing agreement with Sheba Medical Center,” stated Scott Tourville, Chief Executive Officer of ZEUS Scientific, Inc.   “We are hopeful that this new technology will ultimately lead to a portfolio of improved IVD products for the diagnosis of Rheumatoid Arthritis.”

“Prof. Amital and his colleagues developed unique citrullinated peptides composition for the benefit of diagnostic and treatment of Rheumatoid Arthritis (RA), a chronic autoimmune disease, which causes painful inflammation in the joints,” said Sylvie Luria, CEO of Tel Hashomer Medical Research, Infrastructure and Services Ltd. (Tel Hashomer Ltd.).

“We look forward to this collaboration with ZEUS Scientific around this important discovery, which has the potential to revolutionize the diagnosis of Rheumatoid Arthritis,” added Professor Eyal Zimlichman, Sheba Medical Center’s, Chief Medical and Innovation Officer.

The Global Rheumatoid Arthritis (RA) Diagnosis Tests Market is estimated to reach $766.7 million dollars by 2026, while the RA Therapeutics Market was valued at $25.363 billion dollars in 2019 and expected to reach $35.98 billion by 2026.

Hot this week

Cartessa Aesthetics Partners with Classys to Bring EVERESSE to the U.S. Market

Classys, which is listed on the KOSDAQ, is one of South Korea's most distinguished aesthetic technology manufacturers, with devices distributed in 80+ markets globally. This partnership marks Classys's official entry into the American marketplace, with Cartessa Aesthetics as the exclusive distributor for EVERESSE, launched under the Volnewmer brand in current global markets.

Stryker Launches Next-Generation of SurgiCount+

Now integrated with Stryker's Triton technology, SurgiCount+ addresses two key challenges: retained surgical sponges and blood loss assessment. Integrating these previously separate digital solutions provides the added benefit of a more efficient, streamlined workflow for hospitals notes Stryker.

Nevro Receives CE Mark In Europe for It’s HFX iQ™ Spinal Cord Stimulation System

Nevro notes HFX iQ is the first and only SCS system with artificial intelligence (AI) technology that combines high-frequency (10 kHz) therapy built on landmark evidence that uses ongoing cloud data insights to deliver personalized pain relief

Recor Medical Reports: CMS Grants Distinct TPT Device Code and Category to Recor Medical for Ultrasound Renal Denervation

The approval of TPT offers incremental reimbursement payments for outpatient procedures performed with ultrasound renal denervation for Medicare fee-for-service beneficiaries. It becomes effective January 1, 2025, and is expected to remain effective for up to three years notes Recor Medical.

Jupiter Endovascular Reports | 1st U.S. Patient Treated with Jupiter Shape-shifting Thrombectomy Device

“Navigation challenges during endovascular procedures are often underappreciated and have led to under-adoption of life-saving procedures, such as pulmonary embolectomy. We have purpose-built our Endoportal Control technology to solve these issues and make important endovascular procedures accessible to more clinicians and their patients who can benefit from them,” said Carl J. St. Bernard, Jupiter Endovascular CEO. “This first case in the U.S. could not have gone better, and appears to validate the safety and performance we are seeing in our currently-enrolling European SPIRARE I study.”
Exit mobile version