-

PROMETRIKA and Karyopharm: Partners in Global COVID-19 Trial

Cambridge, MA-based clinical research organization to be responsible for Clinical Trial Site Management and On-Site Monitoring in the United States

CAMBRIDGE, Mass.--(BUSINESS WIRE)--PROMETRIKA (www.prometrika.com), a leading clinical research organization, is collaborating with Karyopharm Therapeutics (Nasdaq: KPTI) to conduct the first randomized clinical trial for low-dose selinexor (XPOVIO®), an XPO1 inhibitor, in hospitalized patients with severe COVID-19.

PROMETRIKA will be responsible for US clinical trial site management and on-site monitoring, ensuring collection of accurate and actionable high-quality data. In total, 230 patients will be enrolled into the trial worldwide.

Karyopharm and PROMETRIKA are working closely with investigators and hospital sites at unprecedented speed to accurately capture the data needed to fast-track early findings. The goal is to add to the body of evidence that XPO1 inhibitors may play an important role in treating people with this life-threatening viral infection.

“COVID-19 has accelerated implementation of innovative remote monitoring and data access strategies,” said Heather Paden, Head of Clinical Operations at PROMETRIKA. "Karyopharm's trial is a critical step toward finding effective medicines for those hospitalized due to severe COVID-19 and the PROMETRIKA team is honored to be a part of such an important study."

“We appreciate this opportunity to further contribute to the tireless and comprehensive efforts of our industry in the search for therapeutic tools to combat this horrible pandemic,” said Miganush Stepanians, Founder and CEO at PROMETRIKA.

About PROMETRIKA, LLC - www.prometrika.com
Founded in 2003 and based in Cambridge, Massachusetts, PROMETRIKA is a leading full-service clinical research organization (CRO). Unique in its industry, the company utilizes a caring and collaborative approach to clinical development and execution. They are a cohesive, highly tenured team that prides itself on senior leadership involvement in all phases of a trial. PROMETRIKA’S services include clinical operations, drug safety, medical monitoring, data management, biostatistics and programming, medical writing, and regulatory strategy and submissions. They have collaborated on thousands of studies and helped a wide range of clients achieve new drug approvals by the U.S. FDA and European regulatory authorities.

About Karyopharm Therapeutics, Inc. - www.karyopharm.com.
Karyopharm Therapeutics Inc. (Nasdaq: KPTI) is an oncology-focused pharmaceutical company dedicated to the discovery, development, and commercialization of novel first-in-class drugs directed against nuclear export and related targets for the treatment of cancer and other major diseases. Karyopharm's Selective Inhibitor of Nuclear Export (SINE) compounds function by binding with and inhibiting the nuclear export protein XPO1 (or CRM1). Karyopharm's lead compound, XPOVIO® (selinexor), received accelerated approval from the U.S. FDA in July 2019 in combination with dexamethasone as a treatment for patients with heavily pretreated multiple myeloma. A Marketing Authorization Application for selinexor is also currently under review by the European Medicines Agency. A supplemental New Drug Application was recently accepted by the FDA seeking accelerated approval for selinexor as a new treatment for adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL). SINE compounds have also shown biological activity in models of neurodegeneration, inflammation, autoimmune disease, certain viruses and wound-healing. Karyopharm has several investigational programs in clinical or preclinical development.

Contacts

Deanna Chan, 617-844-0240
dchan@prometrika.com

PROMETRIKA, LLC

NASDAQ:KPTI

Release Summary
Partners in Global COVID-19 Trial
Release Versions

Contacts

Deanna Chan, 617-844-0240
dchan@prometrika.com

Social Media Profiles
More News From PROMETRIKA, LLC

PROMETRIKA Achieves Accreditation in Medidata Rave RTSM

CAMBRIDGE, Mass.--(BUSINESS WIRE)--PROMETRIKA, LLC, is proud to announce it has recently achieved accreditation on Medidata Rave RTSM. Rave RTSM ties subject randomization and management of study drug/supplies directly into the study’s Rave EDC system. This integration streamlines data entry, reduces redundant data entry as compared against separate systems, and allows for mid-stream changes with minimal disruption should study design change. PROMETRIKA’s President and CEO, Miganush Stepanians,...

PROMETRIKA Announces Expanded Strategic Regulatory Consulting Services

CAMBRIDGE, Mass.--(BUSINESS WIRE)--PROMETRIKA, LLC has announced that it has expanded its strategic regulatory consulting services under the leadership of Aileen Ryan, MS, Senior Regulatory Advisor, who has been providing regulatory consulting services to PROMETRIKA’s client companies on a part-time basis for the past 2 years has now joined the company on a full-time basis. Ms. Ryan brings to this position over 40 years of diverse experience in pharmaceutical regulatory affairs, including regul...

Barry Mirrer, Head of Quality Assurance, PROMETRIKA Has Earned CIPP/E Certification

CAMBRIDGE, Mass.--(BUSINESS WIRE)--Barry Mirrer, Head of Quality Assurance, PROMETRIKA, has earned the ANSI-accredited Certified Information Privacy Professional/Europe (CIPP/E) credential through the International Association of Privacy Professionals (IAPP). Mr. Mirrer has been involved with addressing privacy concerns, particularly those related to clinical trials and patient privacy, and providing privacy and security training to organizations for over 15 years. Besides his Quality Assurance...
Back to Newsroom