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Danish listed SaaS IT company opening in South Africa

Loyal Solutions, (NASDAQ: LOYAL) a leading provider of global SaaS loyalty platforms, expands operations to South Africa in order to recruit sufficient IT resources for the ongoing global expansion.

On February 1, we will open our new office in South Africa, yet another step in the globalization of our company.  It will be a big day for Loyal Solutions, and as always this is only possible due to the effort and engagement of the fantastic LS team - a warm thank you to you all.

Peter Kisbye, CEO " As part of our expansion plan, we expect to recruit a significant number of experienced IT developers, and to stay  ahead of the curve we cannot only rely on talent in the Nordics. We selected Johannesburg as our next IT-base, as we find many similarities to the Nordics including a strong educational system with focus on the English language as well as cultures that we are convinced will be a great mix.  Our new IT-hub, puts us in an even stronger position to recruit the right people for the exiting journey we are on "

Our close partner Mortimer Harvey has played an important role in enabling this import step for our company 

Peter Kisbye,CEO
+45 21 28 69 60
pki@loyalsolutions.eu

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Hansa Biopharma completes enrollment in imlifidase phase 2 study in antibody mediated rejection (AMR) episodes post kidney transplantation

  • 30 patients with active or chronic active antibody mediated rejection (AMR) episodes post kidney transplantation have been enrolled and randomized 2:1 to imlifidase v.s. standard-of-care
  • Completion of enrollment marks an important milestone for Hansa, as the company explores the potential of imlifidase in the post transplantation setting. 
  • Acute AMR episodes post kidney transplantation occur in 5-7% of patients, with significant risk of patients losing graft function. There is no approved treatment for preventing and treating AMR. 

Lund, Sweden May 23, 2022. Hansa Biopharma AB, “Hansa”, (Nasdaq Stockholm: HNSA), pioneer in enzyme technology for rare immunological conditions, today announces the completion of enrollment in its phase 2 study evaluating safety, tolerability and efficacy of imlifidase in patients with active and chronic active antibody mediated rejection (“AMR”) episodes. A first data read out is expected in the second half of 2022, as previously guided.

“The on-time completion of enrollment in the AMR phase 2 study is an important milestone in the clinical development of imlifidase for this patient population and is a testimony to our commitment to develop potentially life-saving and life-altering therapies for patients with rare immunological diseases with significant unmet medical need”, says Christian Kjellman, Chief Science Officer, Hansa Biopharma. “Long-term graft survival is challenged by AMR post kidney transplantation, and imlifidase has the potential to have a meaningful positive impact for these patients and the healthcare system at large.”

Acute AMR post kidney transplantation is a serious condition that occurs in 5-7%  of kidney transplants and is a significant challenge to long-term graft survival. AMR, is the main cause of graft dysfunction and loss after kidney transplantation. In the U.S. and Europe, approximately 45,000 patients receive kidney transplants annually, and approximately 400,000, currently live with a kidney transplant.

The AMR phase 2 program is a randomized, open-label, multi-center, controlled study, that has enrolled a total of 30 AMR patients across centers in France, Germany, Austria, Australia, and the U.S. This study is designed to evaluate the safety and efficacy of imlifidase in eliminating donor specific antibodies (“DSAs”) in acute AMR patients, post transplantation. Twenty individuals have been randomized to receive imlifidase treatment comprised of one intravenous dose of 0.25mg/kg, while 10 individuals in the active control arm received 5-10 sessions of plasma exchange. Efficacy and safety is monitored over a six-month period post treatment.

More information about the trial is available at ClinicalTrials.gov under NCT03897205 (2019).

For further information, please contact:
Klaus Sindahl, Head of Investor Relations
Hansa Biopharma 
Mobile: +46 (0) 709-298 269
E-mail: klaus.sindahl@hansabiopharma.com 

Katja Margell
Head of Corporate Communications 
Hansa Biopharma 
Mobile: +46 (0) 768-198 326
E-mail: katja.margell@hansabiopharma.com



Följande bilagor finns för nedladdning:
20220523 HNSA - PR AMR completion of enrollment FINAL ENG

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