New drug DNTH103 aims to tame muscle weakness in myasthenia gravis

NCT ID NCT06282159

First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This Phase 2 study tests a drug called DNTH103 (claseprubart) in 65 adults with generalized myasthenia gravis, a condition that causes muscle weakness. Participants receive either the drug or a placebo, first through an IV and then as injections under the skin every two weeks for 11 weeks. The goal is to see if the drug is safe and can improve daily activities like talking, swallowing, and moving.

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance

Claseprubart (also called DNTH103), a drug given by IV and then injections under the skin

What this could lead to

If it works, this could point toward a new treatment option to control symptoms of generalized myasthenia gravis.

What could go wrong

This is an early Phase 2 trial with only 65 people, so results may not apply to everyone. The drug may not work better than placebo, and side effects are still being studied.

Disclaimer Read more

This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Conditions

The condition(s) this trial relates to.

myasthenia gravis

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Clincal Study Site

    Tampa, Florida, 33620, United States

  • Clinical Study Site

    Phoenix, Arizona, 85028, United States

  • Clinical Study Site

    Irvine, California, 92868, United States

  • Clinical Study Site

    Stamford, Connecticut, 06905, United States

  • Clinical Study Site

    Boca Raton, Florida, 33487, United States

  • Clinical Study Site

    Bradenton, Florida, 34205, United States

  • Clinical Study Site

    Maitland, Florida, 32751, United States

  • Clinical Study Site

    O'Fallon, Illinois, 62269, United States

  • Clinical Study Site

    Kansas City, Kansas, 66103, United States

  • Clinical Study Site

    Lexington, Kentucky, 40503, United States

  • Clinical Study Site

    Boston, Massachusetts, 02215, United States

  • Clinical Study Site

    East Lansing, Michigan, 48824, United States

  • Clinical Study Site

    Columbia, Missouri, 65212, United States

  • Clinical Study Site

    Cincinnati, Ohio, 45219, United States

  • Clinical Study Site

    Columbus, Ohio, 43221, United States

  • Clinical Study Site

    Dallas, Texas, 75206, United States

  • Clinical Study Site

    Dallas, Texas, 75243, United States

  • Clinical Study Site

    Houston, Texas, 77030, United States

  • Clinical Study Site

    Lubbock, Texas, 79414, United States

  • Clinical Study Site

    Richmond, Virginia, 23219, United States

  • Clinical Study Site

    San Miguel de Tucumán, Tucumán Province, T4000, Argentina

  • Clinical Study Site

    Buenos Aires, 20/11/1902, Argentina

  • Clinical Study Site

    Buenos Aires, C1012AAR, Argentina

  • Clinical Study Site

    Buenos Aires, C1015ABR, Argentina

  • Clinical Study Site

    Córdoba, X5004CDT, Argentina

  • Clinical Study Site

    Rosario, 2000, Argentina

  • Clinical Study Site

    London, Ontario, N6A 5W9, Canada

  • Clinical Study Site

    Ostrava, 70852, Czechia

  • Clinical Study Site

    Copenhagen, 02100, Denmark

  • Clinical Study Site

    Bordeaux, 33076, France

  • Clinical Study Site

    Nice, 06001, France

  • Clinical Study Site

    Strasbourg, 67000, France

  • Clinical Study Site

    Haifa, 3109601, Israel

  • Clinical Study Site

    Ramat Gan, Israel

  • Clinical Study Site

    Safed, 13100, Israel

  • Clinical Study Site

    Milan, 20133, Italy

  • Clinical Study Site

    Naples, 80131, Italy

  • Clinical Study Site

    Pisa, 56126, Italy

  • Clinical Study Site

    Rome, 00168, Italy

  • Clinical Study Site

    Rome, 00189, Italy

  • Clinical Study Site

    Amsterdam, Netherlands

  • Clinical Study Site

    Skopje, 1000, North Macedonia

  • Clinical Study Site

    Bergen, 5021, Norway

  • Clinical Study Site

    Bydgoszcz, 85-065, Poland

  • Clinical Study Site

    Katowice, 40123, Poland

  • Clinical Study Site

    Krakow, 31-202, Poland

  • Clinical Study Site

    Krakow, 31-503, Poland

  • Clinical Study Site

    Lublin, 20-093, Poland

  • Clinical Study Site

    Warsaw, 01-684, Poland

  • Clinical Study Site

    Warsaw, 02-657, Poland

  • Clinical Study Site

    Belgrade, 11000, Serbia

  • Clinical Study Site

    Kragujevac, 34000, Serbia

  • Clinical Study Site

    Niš, 18000, Serbia

  • Clinical Study Site

    Novi Sad, 21000, Serbia

  • Clinical Study Site

    Malmö, Sweden

  • Clinical Study Site #2

    Houston, Texas, 77030, United States