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4 articles from the last 90 days matching "europe"

Clinical trialRSS4 days ago

Trial testing safety, effectiveness of add-on PH treatment kicks off

A company called Allrock Bio is testing a new oral medication called ROC-101 for pulmonary hypertension (a condition where blood pressure in the lungs becomes dangerously high). This is a Phase 2a trial, which means they're checking if the drug is safe and works well as an add-on treatment. The trial is now enrolling patients across the U.S., Canada, and Europe.

WHY IT MATTERSIf ROC-101 proves effective as an add-on therapy, it could offer pulmonary hypertension patients a new oral option to combine with their existing treatments, potentially improving symptom control.
You can act on thispulmonary hypertensionRead →
Clinical trialCLINICALTRIALSApr 3

Trial Now Recruiting: The Head and Neck Registry of the European Reference Network on Rare Adult Solid Cancers (NCT05483374)

Doctors across Europe are building a database to track rare head and neck cancers like nasopharynx cancer and salivary gland cancer. They're recruiting 13,600 patients to help them understand how these cancers develop and improve treatment. This registry will help researchers learn more about these uncommon cancers so doctors can treat patients better in the future.

WHY IT MATTERSIf you have a rare head and neck cancer like nasopharynx or salivary gland cancer, joining this registry helps European specialists understand your condition better and could improve treatment options for patients like you.
💬 Ask your doctorNasopharynx cancerNasal cavity and paranasal sinus cancerSalivary gland cancerRead →
Clinical trialCLINICALTRIALSMar 27

Trial Now Recruiting: A Pilot Study to Assess the Feasibility and Acceptability of Newborn Screening Using in Silico Panel-based Solo Genome Sequencing in France (NCT06875089)

Researchers in France are recruiting 5,000 newborns to test a new way of screening for rare diseases using genome sequencing—a complete reading of a baby's DNA. Instead of the current blood spot tests that check for only a few dozen conditions, this study will see if reading a baby's entire genome can safely and effectively find many more rare genetic diseases at birth. This is one of the first major studies in Europe to test this approach.

WHY IT MATTERSThis trial could expand newborn screening in France to detect dozens of additional rare genetic diseases at birth, potentially allowing earlier treatment and better health outcomes for babies with conditions that currently go undiagnosed until symptoms appear.
You can act on thisRare genetic diseases detectable at birthConditions currently missed by standard newborn screeningRead →
Clinical trialCLINICALTRIALSMar 26

New Clinical Trial: New Analytic Tools for aHUS and C3G Diagnosis (NCT05985122)

Researchers across 7 European countries are working together to develop better ways to diagnose two rare kidney diseases: atypical hemolytic-uremic syndrome (aHUS) and C3 glomerulonephritis (C3G). This study is enrolling 180 people, including patients with these conditions and healthy volunteers, to test new diagnostic tools that could help doctors identify these diseases more quickly and accurately.

WHY IT MATTERSThis trial is developing improved diagnostic tests for aHUS and C3G, which could help patients get diagnosed faster and start treatment sooner—critical since these complement-mediated kidney diseases can cause permanent kidney damage if left untreated.
Good to knowAtypical Hemolytic-Uremic Syndrome (aHUS)C3 Glomerulonephritis (C3G)Membranoproliferative GlomerulonephritisRead →

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