Cystic Fibrosis Foundation

- Country
- 🇺🇸United States
- Ownership
- Private
- Established
- 1955-01-01
- Employees
- 501
- Market Cap
- -
- Website
- http://www.cff.org
Clinical Trials
1
Trial Phases
1 Phases
Drug Approvals
0
Drug Approvals
No drug approvals found
This company may not have drug approvals in our database
Clinical Trials
Distribution across different clinical trial phases (1 trials with phase data)• Click on a phase to view related trials
Zinc Homeostasis and Kinetics in Children With Cystic Fibrosis (CF)
- First Posted Date
- 2005-03-02
- Last Posted Date
- 2015-07-30
- Lead Sponsor
- Cystic Fibrosis Foundation
- Target Recruit Count
- 30
- Registration Number
- NCT00104494
- Locations
- 🇺🇸
Baylor College of Medicine, Houston, Texas, United States
News
4DMT Secures $11 Million CF Foundation Investment to Advance Gene Therapy 4D-710 into Phase 2 for Cystic Fibrosis
The Cystic Fibrosis Foundation will provide up to $11 million in additional funding to 4D Molecular Therapeutics to accelerate development of 4D-710, a gene therapy for cystic fibrosis lung disease.
ReCode Therapeutics Secures $29M Financing to Advance Inhaled mRNA Therapy for Cystic Fibrosis
ReCode Therapeutics raised over $29 million in additional financing to advance its genetic medicines pipeline, including investigational therapies for cystic fibrosis.
Cystic Fibrosis Foundation Commits Additional $24 Million to Prime Medicine for Gene Editing Therapy Development
The Cystic Fibrosis Foundation has committed up to $24 million in additional funding to Prime Medicine to advance prime editing gene therapy for cystic fibrosis patients.
Cystic Fibrosis Foundation Invests $2.3 Million in Owlstone Medical to Develop Breath-Based Pathogen Test
Owlstone Medical has secured a $2.3 million equity investment from the Cystic Fibrosis Foundation to develop a breath test for detecting Pseudomonas aeruginosa infections in CF patients.
AbbVie and Galapagos Form $406 Million Alliance to Develop Novel Cystic Fibrosis Therapies
• AbbVie has partnered with Galapagos NV in a global alliance worth up to $406 million to discover and develop combination therapies targeting key mutations in cystic fibrosis patients. • The collaboration aims to develop oral drugs addressing F508del and G551D mutations in the CFTR protein, with plans to initiate Phase 1 clinical trials by the end of 2014. • This partnership joins other significant industry efforts to combat cystic fibrosis, including Pfizer's expanded six-year research program with the Cystic Fibrosis Foundation worth up to $58 million.
Cystic Fibrosis Foundation Invests $15 Million in Recode Therapeutics for CF Gene Editing
• The Cystic Fibrosis Foundation is investing $15 million in Recode Therapeutics to advance gene-editing medicines for cystic fibrosis (CF) patients without effective treatment options. • Recode Therapeutics collaborates with Intellia Therapeutics, developing a strategy to alter the genetic code, creating a healthy CFTR gene version for functional protein production. • The funding supports the development of up to three gene-correction programs, initially focusing on CF mutations not addressed by existing therapies. • Recode's RCT2100, an inhaled mRNA therapy delivering a healthy CFTR version to lung cells, is currently in Phase 1 clinical trials, expanding treatment options for all CF patients.
RDCA-DAP Boosts Cystic Fibrosis Research with New Data Sets
The RDCA-DAP has acquired new datasets from the Cystic Fibrosis Therapeutics Development Network to accelerate cystic fibrosis (CF) research and therapy development.
