The purpose of our Phase 2 trial, TRACTION-2, is to determine if our once-daily, oral, investigational precision medicine, GFB-887, is beneficial for people with high levels of protein in their urine due to focal segmental glomerulosclerosis (FSGS), diabetic nephropathy (DN) or treatment resistant minimal change disease (TR-MCD).
To learn more about TRACTION-2, visit TractionClinicalTrial.com or clinicaltrials.gov
Because of the current lack of therapeutic options, many people with kidney disease follow the same trajectory. They progress from disease onset to end-stage kidney disease and, ultimately, dialysis and transplantation, significantly impacting their quality of life.
The halo symbolizes our goal to protect people with kidney disease from following this path by delivering disease-modifying precision medicines.
Learn more about some of the organizations working on behalf of you and your loved ones:
It is our duty to carefully evaluate the safety and efficacy of any of our investigational precision medicine product candidates. We believe that clinical trials are the best and most appropriate way to do that. The process is a collaborative effort, and we will work closely with researchers, physicians, clinical trial site teams, people living with kidney diseases and their families to conduct our studies efficiently and effectively. When successful, data from these studies form the basis of regulatory (i.e. U.S. Food and Drug Administration, European Medicine Agency, or other similar regulatory agencies) approvals, which ensure the most equitable and sustainable access to our precision medicines for the people who need them.
We know that people living with kidney diseases and their families are counting on us to potentially extend and improve their quality of life. Given this, we understand that some people living with kidney diseases and their families may be interested in accessing our investigational precision medicine product candidates prior to regulatory approval, and outside of the clinical trial setting, through an expanded access program (sometimes referred to as “early access” or “compassionate use”). Goldfinch Bio does not offer programs that allow access to our precision medicine product candidates prior to regulatory approval. For now, participating in a clinical trial is the only way to access our precision medicine product candidates.
More information about Goldfinch Bio’s current clinical trials is available above in the section titled “Information about our ongoing clinical trials.” If you have additional questions, please talk to your doctor or contact earlyaccessprogram@goldfinchbio.com. We plan to acknowledge receipt of requests sent to this email address within five business days.
FSGS is a rare disease that attacks the kidney’s glomerulus and podocytes, causing scarring that leads to permanent kidney damage.
DN is a complex and heterogeneous complication of diabetes with numerous overlapping disease-causing pathways.