Myasthenia Gravis Drug Gets FDA Nod

Argentina Noticias Noticias

Myasthenia Gravis Drug Gets FDA Nod
Argentina Últimas Noticias,Argentina Titulares
  • 📰 Medscape
  • ⏱ Reading Time:
  • 10 sec. here
  • 2 min. at publisher
  • 📊 Quality Score:
  • News: 7%
  • Publisher: 55%

The monoclonal antibody rozanolixizumab (Rystiggo) is indicated to treat adults with the two most common subtypes of generalized myasthenia gravis.

who are positive for anti-acetylcholine receptor or anti-muscle-specific tyrosine kinase antibody, the drug's manufacturer, UCB, has announced.

Rozanolixizumab is a subcutaneous-infused humanized IgG4 monoclonal antibody that binds to the neonatal Fc receptor , reducing the concentration of pathogenic IgG autoantibodies.

Hemos resumido esta noticia para que puedas leerla rápidamente. Si estás interesado en la noticia, puedes leer el texto completo aquí. Leer más:

Medscape /  🏆 386. in US

Argentina Últimas Noticias, Argentina Titulares

Similar News:También puedes leer noticias similares a ésta que hemos recopilado de otras fuentes de noticias.

FDA approves 1st treatment that can grow back hair for teens with severe alopecia areataFDA approves 1st treatment that can grow back hair for teens with severe alopecia areataMarking a historic first, the FDA has approved an alopecia treatment for kids 12 and over.
Leer más »

Experimental drug could offer more weight loss than any drug now on the market, study findsThe experimental drug, retatrutide, helped people lose, on average, about 24% of their body weight, the equivalent of about 58 pounds, in a mid-stage clinical trial, the company says.
Leer más »

Scientists reworked an experimental cancer therapy to treat autoimmune diseaseThe experimental cancer treatment was reworked, using RNA engineering, to address an autoimmune disorder called myasthenia gravis.
Leer más »

Hydration nation: Clients clamor for IV therapy on demand even though it’s not FDA-approvedAre IV therapy 'bars' and stations worth all the hype? Fox News Digital spoke to multiple experts about the benefits and risks of these on-demand hydration facilities.
Leer más »

Dublin family celebrates FDA approval of gene therapy for Duchenne developed in Central Oh'It is huge. It’s going to change the course of this disease,' said Dublin mom Amber Nisley. 'I mean, it truly is a game changer. This has never happened before
Leer más »

AC Immune’s stock soars 13% after FDA grants fast-track designation to Alzheimer’s treatmentAC Immune SA’s stock soared 13% premarket Tuesday, after the Swiss-based biotech said it has received U.S. Food and Drug Administration fast-track...
Leer más »



Render Time: 2025-04-18 08:47:18