X
Pharma Advancement
  • Home
  • Articles
  • Drug Development
    • All
    • Clinical Trials
    • FDA Approvals
    • Research & Development
    Merck to Acquire Verona

    Merck to Acquire Verona Pharma in $10B Deal Boosts COPD Drug

    Emerging Oral Small Molecule Drugs

    Emerging Oral Small-Molecule Drugs for Ultra-Rare Diseases

    FDA Approves Oral Therapy for Treating Hereditary Angioedema

    FDA Approves Oral Therapy for Treating Hereditary Angioedema

    Avadel Pharmaceuticals Receives

    Avadel Pharmaceuticals Receives Orphan Drug Designation from FDA for LUMRYZ™ (sodium oxybate) for Extended-Release Oral Suspension for the Treatment of Idiopathic Hypersomnia

    Robots and AI in Drug

    Robots and AI in Drug Discovery Are Transforming Medicine

    Stringent Policy around COVID Vaccines Laid by FDA

    Stringent Policy around COVID Vaccines Laid by FDA

    Pharmaceutical-Chemicals Market Booms with Rising API Demand

    Pharmaceutical Chemicals Market Booms with Rising API Demand

    Next in Pharma 2025 Innovations

    Next in Pharma 2025: Innovations Shaping the Future

    Work Smart: Go for Hands-Free Lab Informatics at the Bench, Not Scribbled Notes and Delayed Documentation at Your Desk

  • Manufacturing
  • Supply Chain
  • Facilities
  • Insights
  • Events
  • Contact Us
No Result
View All Result
  • Home
  • Articles
  • Drug Development
    • All
    • Clinical Trials
    • FDA Approvals
    • Research & Development
    Merck to Acquire Verona

    Merck to Acquire Verona Pharma in $10B Deal Boosts COPD Drug

    Emerging Oral Small Molecule Drugs

    Emerging Oral Small-Molecule Drugs for Ultra-Rare Diseases

    FDA Approves Oral Therapy for Treating Hereditary Angioedema

    FDA Approves Oral Therapy for Treating Hereditary Angioedema

    Avadel Pharmaceuticals Receives

    Avadel Pharmaceuticals Receives Orphan Drug Designation from FDA for LUMRYZ™ (sodium oxybate) for Extended-Release Oral Suspension for the Treatment of Idiopathic Hypersomnia

    Robots and AI in Drug

    Robots and AI in Drug Discovery Are Transforming Medicine

    Stringent Policy around COVID Vaccines Laid by FDA

    Stringent Policy around COVID Vaccines Laid by FDA

    Pharmaceutical-Chemicals Market Booms with Rising API Demand

    Pharmaceutical Chemicals Market Booms with Rising API Demand

    Next in Pharma 2025 Innovations

    Next in Pharma 2025: Innovations Shaping the Future

    Work Smart: Go for Hands-Free Lab Informatics at the Bench, Not Scribbled Notes and Delayed Documentation at Your Desk

  • Manufacturing
  • Supply Chain
  • Facilities
  • Insights
  • Events
  • Contact Us
No Result
View All Result
Pharma Advancement
No Result
View All Result
Home Drug Development

Rare Illnesses: mRNA Therapy May Swap Intracellular Proteins

Content Team by Content Team
13th April 2024
in Drug Development, News
AstraZeneca Forges RNA-Modifying Protein Oncology Deal with Accent Therapeutics

Note* - All images used are for editorial and illustrative purposes only and may not originate from the original news provider or associated company.

Notably, the interim data from a Phase I/II clinical trial goes on to suggest that mRNA-3927, which happens to be an investigational mRNA therapy from Moderna, can very well be a promising treatment when it comes to propionic acidaemia.

A 70% reduction in terms of risk of metabolic decompensation events had been reported by eight participants across the 12-month pretreatment period, as per the trial results published in Nature.

They are excited to share the first published clinical data by way of using an mRNA therapy for intracellular protein replacement, stated Moderna’s Senior Vice President as well as Head of Development, Therapeutics, and Oncology, Dr. Kyle Holen.

A novel mRNA therapy

mRNA-3927 happens to be a novel lipid nanoparticle- LNP and is an encapsulated dual investigational mRNA therapy. By encoding for the PCC enzyme. It happens to have the potential to replace missing or dysfunctional enzymes, stated the pharmaceutical giant.

Propionic acidaemia is indeed rare and is an inherited metabolic disorder that goes on to result from the body’s inability to go ahead and process specific parts of proteins as well as lipids because of a specific enzyme deficiency. For people with propionic acidaemia, harmful levels of toxic metabolites can build up in the body and can as well lead to metabolic decompensation events as well as multisystemic complexities. These interim data go on to indicate early signs of potential clinical benefit by way of having mRNA-3927 and significantly also demonstrate that mRNA-3927 happens to have an infrequent treatment, limiting the side effects. Dr. Holen said that he is particularly proud of such kind of results given that there happen to be at present no therapeutic treatments that are approved for patients with this disease.

It is well to be noted that the company’s ongoing global Phase I/II clinical trial evaluated the safety, pharmacodynamics, and pharmacokinetics of the IV-administered treatment in participants aged one year and above. Study data happened to be presented at the 2023 American Society of Gene & Cell Therapy- ASGCT Yearly Meeting.

The fact is that as of the latest data cutoff at May 2023 end, more than 15 person-years of therapy were administered.

Moderna confirmed that additional patient enrollment when it comes to dose expansion phase of the study will go on to further assess the efficacy, safety, and pharmacodynamic activity of mRNA-3927.

Apparently, in the week ending March 30, 2024, Moderna went on to share promising data for its next-generation COVID-19 vaccine.

Previous Post

LAI Antipsychotic - Given The Green Light Across The EU

Next Post

Lab Bottlenecks? Digitalized Lab Management Systems Can Help

Related Posts

Merck to Acquire Verona
Drug Development

Merck to Acquire Verona Pharma in $10B Deal Boosts COPD Drug

21st July 2025
ChiRhoClin LogiCare3PL Partners for Drug Distribution
News

ChiRhoClin, LogiCare3PL Partners for Drug Distribution

21st July 2025
Emerging Oral Small Molecule Drugs
Drug Development

Emerging Oral Small-Molecule Drugs for Ultra-Rare Diseases

21st July 2025
Thermo Fisher and Sanofi Partners
Manufacturing

Thermo Fisher and Sanofi Partners for US Drug Manufacturing

21st July 2025
EMA Recommendations to Secure Anti D Immunoglobulins Supply
News

EMA Recommendations to Secure Anti-D Immunoglobulins Supply

15th July 2025
FDA Approves Oral Therapy for Treating Hereditary Angioedema
FDA Approvals

FDA Approves Oral Therapy for Treating Hereditary Angioedema

15th July 2025
Next Post
Thermo Fisher Scientific Announces Collaboration with Northeastern University to Advance Biopharmaceutical Characterization and Monitoring Workflows

Lab Bottlenecks? Digitalized Lab Management Systems Can Help

Qucik Links

  • Drug Development
  • Manufacturing
  • News
  • Events & Conferences
  • Newsletter Archive
Pharma Advancement

About Us

Pharma Advancement is a leading Pharma information centric website. On one side Pharmaadvancement.com has established itself as one of the most efficient and comprehensive source of Pharma information online, dedicated to providing decision makers in all the Pharma industry sectors with reliable, accurate and useful insights into happenings in the Pharma sector.

Subscribe Us

System

  • Search
  • Sitemap
  • RSS Feed

Resources

  • Advertise with us
  • Contact Us
  • Download Mediapack
  • Newsletters Archive

© 2017 Copyright © Valuemediaservices 2017 All rights reserved.

No Result
View All Result
  • Home
  • Articles
  • Drug Development
  • Manufacturing
  • Supply Chain
  • Facilities
  • Insights
  • Events
  • Contact Us

© 2017 Copyright © Valuemediaservices 2017 All rights reserved.

Login to your account below

Forgotten Password?

Fill the forms bellow to register

All fields are required. Log In

Retrieve your password

Please enter your username or email address to reset your password.

Log In