eRapa (encapsulated rapamycin) Named Patient Programme

Investigational – Not Approved

Supporting Access for Patients with Familial Adenomatous Polyposis (FAP)

Biodexa Pharmaceuticals is committed to advancing new therapies for rare diseases with significant unmet medical need. Where appropriate and permitted by local regulations, Biodexa supports early accessprogrammes to enable eligible patients to access investigational medicines outside of clinical trials.

About the Programme

The eRapa Named Patient Programme has been established to provide access to eRapa, an investigational oral formulation of rapamycin, for certain patients diagnosed with Familial Adenomatous Polyposis (FAP).

The programme is intended for patients:

  • With serious or life‑threatening disease
  • Who are unable to participate in a clinical trial
  • For whom the treating physician believes treatment may be appropriate

Access is subject to local regulatory and legal requirements, medical eligibility andprogramme criteria, product availability, and applicable funding mechanisms.

model of colon
grandparents and family smiling

About Familial Adenomatous Polyposis

Familial Adenomatous Polyposis is a rare inherited condition characterized by the development of multiple colorectal polyps, often beginning in adolescence. If untreated, FAP is associated with a high risk of colorectal cancer. Currently, there are no approved pharmacological therapies, and surgical intervention remains the standard of care in many patients.erenta trial is a Phase 3 clinical trial for people diagnosed with familial adenomatous polyposis (FAP). The purpose of this trial is to test an experimental treatment, eRapa, to evaluate its ability to improve clinical outcomes in FAP patients vs placebo (inactive substance).

About eRapa

eRapa is a proprietary oral capsule formulation of rapamycin (sirolimus). Rapamycin inhibits the mTOR pathway, which plays a role in cellular growth and proliferation and has been shown to be over‑expressed in FAP‑associated polyps.

eRapa is an investigational medicine that is currently being evaluated in clinical trials and has not been approved by any regulatory authority. Its clinical benefits and risks have not yet been fully established.

Programme Oversight

The eRapa Named Patient Programme is available on a case‑by‑case basis, requires requests to be submitted by a licensed treating physician, and is implemented in collaboration with Tanner Pharma Group, which provides compliant, controlled access services globally.

Contact Information

For information related to the eRapa Named Patient Programme, healthcare providers may contact:

Email: erapa@tannerpharma.com

doctors consultation

Important Notice

This programme is not intended to replace participation in clinical trials where such participation is feasible. Biodexa may modify or discontinue the programme in accordance with applicable regulations.