NextCell to present its progress at Swiss Nordic Bio 2020

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NextCell Pharma AB ("NextCell") presented, in December 2019, efficacy data of ProTrans stem cells in an interim analysis of the ongoing phase I/II trial, ProTrans-1. Patients receiving medium or high dose of ProTrans showed a statistically significant effect as compared to low dose. The company will present data at Swiss Nordic Bio 2020, on February 6 in Zurich.

Swiss Nordic Bio is a partnering and investor conference aimed at connecting healthcare innovations, investors and industry. For NextCell this is an opportunity to inform international investors and potential collaborators about developments and future goals. NextCell has received funding and support from Vinnova and Business Sweden to attend the event.

NextCell Pharma is currently running two parallel trials with ProTrans for the treatment of patients with type 1-diabetes.  The first trial is ProTrans-1, a two-part phase I/II trial design assessing the safety and efficacy of the study drug. In the first part, a dose escalation with three patients in 3 dose cohorts is used to evaluate the safety. An interim analysis of patients in the first part receiving medium or high dose of ProTrans showed a statistically significant effect as compared to low dose.  The second part includes 15 patients that are randomized to active treatment or placebo (2:1 ratio), both patients and investigators are blinded. Topline data from the phase II part is expected to be available in the third quarter 2020.

The second clinical trial, ProTrans-Repeat, started in Maj 2019 and is a Phase IIa clinical trial that aims to evaluate whether repeated treatment can increase or maintain the effect of ProTrans over a longer period of time while maintaining safety. The effect is measured by comparing the patient’s ability to produce insulin before treatment, with twelve months after treatment with the repeated dose of ProTrans. This trial includes a maximum of eighteen patients, of which nine already received active treatment and the other patients will act as the control group. All patients receiving active treatment with ProTrans have previously been treated in the ProTrans-1 study’s dose escalation phase and are now about to receive repeated treatment in the ProTrans-Repeat trial. The patients in the control group have not, and will not, receive treatment with ProTrans, but are followed to compare the natural course of diabetes with how the disease develops during treatment with ProTrans.

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LinkedIn: https://www.linkedin.com/company/15255207/

Twitter: https://twitter.com/NextCellPharma

For more information about NextCell Pharma AB, please contact:

Mathias Svahn, CEO

Sofia Fredrikson, CFO

Phone: 08-735 5595

E-mail: info@nextcellpharma.com

www.nextcellpharma.com

About NextCell Pharma AB:

Stem cells are expected to change the way how many of today's life-threatening diseases are treated. NextCell

Pharma AB develops ProTrans, a drug candidate consisting of stem cells for the primary treatment of autoimmune and inflammatory diseases as well as for use in kidney transplants. ProTrans consists of selected stem cells derived from the umbilical cord tissue with NextCell's patent pending selection algorithm. NextCell operates the stem cell bank Cellaviva, which is Sweden's first and only IVO-approved biobank for family-saving of stem cells from umbilical cord blood and umbilical cord tissue.

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