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CNP-106 Clinical Trial Myasthenia Gravis

PURPOSE

The main aim of this study is to see how safe and tolerable CNP-106, an investigational drug, is for people with Myasthenia Gravis.  The study will  help determine if CNP-106 can help improve your MG symptoms by reprogramming your immune system. All participants will receive CNP-106 or Placebo intravenously on Day 1, Day 8, and for some Day 90.

Key Inclusion Requirements

  • Men and Women ages 18-75 years old
  • Positive test for antibodies to acetylcholine receptors
  • Myasthenia Gravis Foundation of America Clinical Classification Class III-IV

Key Exclusion Requirements

  • Myasthenia Gravis Foundation of America Clinical Classification Class I or Class V
  • If you have received a COVID-19 vaccine within 14 days of screening or are planning to receive any vaccination during your time on the study

Active Clinical Sites

Barrow Neurological Institute

Phoenix, AZ

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Contact: Katherine Podsiadlo
Email: katherine.podsiadlo@dignityhealth.org

Infusion for Health

Brea, CA

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Contact: Danielle Mendoza
Phone: (1) 626-536-8974
Email: damendoza@infusionforhealth.com

University of California, Irvine

Orange, CA

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Contact: Dana Tran
Phone: (1) 714-509-2117
Email: danat2@hs.uci.edu

University of California Davis

Sacramento, CA

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Contact: Becky Craig
Email: rscraig@ucdavis.edu

Yale University

New Haven, CT

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Contact: Katerina Palma
Phone: (1) 612-594-4080
Email: katerina.palma@yale.edu

Atlantis Clinical Research

Miami, FL

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Contact: Laritza Lincheta Enriquez
Phone: (1) 786-536-7779
Email: llincheta@atlantisclinicalresearch.com

Quantix Research

Miami, FL

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Contact: Ryan Vespe
Phone: (1) 305-230-7371
Email: ryan.vespe@quantixresearch.com

University of South Florida

Tampa, FL

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Contact: Alexis Flores
Phone: (1) 813-974-9752
Email: aflores11@usf.edu

Insight Research Institute Chicago

Chicago, IL

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Contact: Ibrahim Mahgoub
Phone: (1) 312-567-6675
Email: Ibrahim.mahgoub@iinn.com

University of Kansas Medical Center

Kansas City, KS

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Contact: Abby Davis
Phone: (1) 913-945-9934
Email: adavis54@kumc.edu

Insight Research Institute Dearborne

Dearborn, MI

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Contact: Albaraa Alkilani
Phone: (1) 810-275-1964
Email: albaraa.alkilani@iinn.com

University of Missouri

Columbia, MO

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Contact: Neetha Gali
Phone: (1) 573-882-3065
Email: ngdcd@health.missouri.edu

Ohio State University Wexner Medical Center

Columbus, HO

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Contact: Karim Kheniser
Email: Karim.Kheniser@osumc.edu

Medical University of South Carolina

Charleston, SC

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Contact: Alison Vance Line
Phone: (1) 843-792-2845
Email: line@musc.edu

Nerve and Muscle Center of Texas

Houston, TX

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Contact: Amy Megerle
Phone: (1) 713-795-0033 ext. 14
Email: houneuamy@msn.com

Prolato Clinical Research

Houston, TX

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Contact: Romeo Parada
Phone: (1) 832-338-9118
Email: rparada@prolato.org

Virginia Commonwealth University

Richmond, VA

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Contact: Taylor Parkinson
Phone: (1) 804-832-1390
Email: taylor.parkinson@vcuhealth.org

How many participants are being enrolled?

The number of total participants to be enrolled in the clinical trial.

Approximately 54 participants across about 40 centers in the US.

Are placebos part of the clinical trial?

A placebo often looks like the investigational medication but has no active ingredient in it. It is used to compare against the actual investigational treatment to evaluate effectiveness.

Yes, participants will receive an infusion of either CNP-106 therapy or placebo (salt water).

How long is participation in the clinical trial?

The planned length of time each participant will take part in the clinical trial.

~180 days: including active study participation and follow-up period.

Clinicaltrials.gov

Clinical Trial Identifier

A Clinical Trial Identifier is a unique number assigned to a clinical trial by clinical trial registries around the world.

NCT06106672

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