UNION Therapeutics Announces Expansion of Clinical Pipeline: Adds UNI91103 to Prevent COVID-19 and Reduce the Severity of the Diseases Among Those Already Infected

October 10, 2020

UNION therapeutics A/S announces expansion of the clinical pipeline with the addition of UNI91103 (intranasal niclosamide) to prevent COVID-19 and reduce the severity of the diseases among those already infected.

An alternative to vaccination in high-risk groups

Several high-risk patient groups do not respond well to vaccination suggesting a persistent need for alternative prophylactic measures. In response, UNION has expanded its clinical program for COVID-19 with a niclosamide based nasal spray (UNI91103) to prevent and alleviate infection among people at risk. UNI91103 will first be investigated in high risk patients to test its ability to prevent infection with COVID-19 and to reduce the severity of the disease for those already infected.

In addition, the nasal spray will be used in the treatment trials in combination with UNION’s inhalation product (UNI91104), which continues development for treatment of COVID-19. The nasal spray product, UNI91103, has been successfully tested in 44 healthy volunteers without significant safety concerns and is ready for tests in COVID-19 patients as well as subjects at risk of contracting COVID-19.

Maximizing the likelihood of prevention and treatment options

“The split of our COVID-19 program into two independent products for treatment and prevention of COVID-19 substantially increases the likelihood of bringing aid to patients and reducing societal impact” says Rasmus Toft-Kehler, CEO and co-founder of UNION.

Niclosamide was recently identified by Institut Pasteur Korea as a potent inhibitor of SARS-CoV-2, the virus causing COVID-191. Furthermore, niclosamide has been demonstrated to prevent fatal outcomes in a murine model of COVID-19 when administered intranasally2.

Studies have documented that SARS-CoV-2 replicates most rapidly in the nasal epithelial cells and suggest that initial replication of the virus in the nasal cavity then leads to infection of the lungs. Sinonasal pathophysiology is increasingly important for our understanding of COVID-19, and the sinonasal tract is thought to be an important site for both infection as well as transmission3.

“The sinonasal cavity is an important site for the establishment and replication of SARS-CoV-2 in the early stages of COVID-19, accordingly we consider delivery of niclosamide directly to this site of early infection a key strategy for limiting the infection of people otherwise at risk for contracting COVID-19,” says UNION co-founder Professor Morten Sommer. UNION therapeutics expects to commence patient trials using UNI91103 in Q4 2020.


References

  1. Jeon et al. AAC 2020, DOI: 10.1128/AAC.00819-20
  2. Brunaugh et al. BiorXiv 2020, DOI: 10.1101/2020.09.24.310490
  3. Gengler et al. Laryngoscope Investig Otolaryngol  2020, DOI: 10.1002/lio2.384

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.”