🏛️ Verified NIH Record • Updated 2026-07-21

PHENOGENE-1A (Cromolyn) Treatment in Patients With Mild to Moderate ALS (NCT07142291)

A Phase IIB Randomized, Double-Blind, Placebo-Controlled, Multi-Dose Study to Evaluate the Effects of PHENOGENE-1A (Cromolyn) as an Adjuvant Treatment in Subjects With Mild to Moderate Amyotrophic Lateral Sclerosis (ALS)

🟢 Recruiting Phase2 💊 Investigational Drug / Biologic Sponsor: PhenoNet, Inc.

🩺 Plain-English Summary (8th-Grade Level)

The purpose of this study is to test the effects of PHENOGENE-1A, which is the treatment under investigation in this study. This research will investigate if PHENOGENE-1A can help people with ALS by measuring their function using the ALS Functional Rating Scale Revised (ALSFRS-R), measuring lung function using pulmonary function tests (PFTs), such as forced vital capacity (FVC), and measuring neuro-inflammatory biomarkers in the blood.

Who can join: Review the eligibility criteria below.

Location: Honor Health Neurology - Bob Bove Neuroscience Institute — Scottsdale, Arizona

Age range: 18 Years to 75 Years

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (22 Sites)

  • Honor Health Neurology - Bob Bove Neuroscience Institute — Scottsdale, Arizona
  • University of California San Diego — La Jolla, California
  • Sutter Health - California Pacific Medical Center Research Institute — San Francisco, California
  • Mayo Clinic Jacksonville — Jacksonville, Florida
  • Lange Neurology — New York, New York
  • NEUROHK s.r.o. — Hradec Králové,
  • Fakultni Nemocnice Hradec Kralove — Hradec Králové,
  • Thomayer University Hospital - Fakultni Thomayerova nemocnice — Prague,
  • Charité Centrum für Neurologie, Neurochirurgie und Psychiatrie — Berlin,
  • DIAKOVERE Henriettenstift - Klinik für Neurologie und Klinische Neurophysiologie — Hanover,
  • Universitaetsklinikum Schleswig-Holstein — Lübeck,
  • Michalski i Partnerzy Lekarze Spółka Partnerska — Krakow,
  • SP ZOZ Szpital Uniwersytecki w Krakowie — Krakow,
  • Centrum Medyczne NeuroProtect (NeuroProtect Medical Center) — Warsaw,
  • City Clinic Research — Warsaw,
  • University Clinical Center of Serbia — Belgrade,
  • Hospital General Universitario Dr. Balmis de Alicante — Alicante,
  • Barcelona Sea Hospital (Hospital Del Mar De Barcelona) — Barcelona,
  • Hospital Universitario Vall D Hebron — Barcelona,
  • Hospital Universitario Ramon Y Cajal — Madrid,
  • Hospital Regional Universitario De Malaga — Málaga,
  • Hospital Universitario Virgen Del Rocio — Seville,

📞 Contact the Study Coordinator

Phone: (617) 784-0490

Email: delmaleh@phenonet.us

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

💰 Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

💡 How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
🏛️ View Official NIH Record ↗