Patients & Families

At Feldan Therapeutics, we focus on developing new treatments that address unmet medical needs and truly make a difference for people living with skin and lung conditions.

This page provides patients and families general information about these conditions, as well as insights into our innovative therapies and the ways they are developed — presented in an informative and supportive manner, while never replacing personalized medical advice.

Basal Cell Carcinoma

FLD-103 for Basal Cell Carcinoma

FLD-103 is a non-surgical therapy designed to target basal cell carcinoma through local injection directly into the tumor. Currently being investigated in a Phase 1/2a clinical trial, FLD-103 is developed to minimize scarring and reduce the impact of repeated surgeries. 

Mucus-Driven Diseases

FLD-201 for Mucus-Driven Diseases

FLD-201 is an inhalation therapy for mucus-driven lung diseases, designed to address the underlying mechanism of excess mucus build-up and help improve breathing and quality of life for patients living with chronic lung conditions. FLD-201 is currently in the preclinical development phase. 

How Does a Medicine Reach Patients?

 A clinical trial is a critical step in the development of new medicines. It is designed to evaluate the safety and effectiveness of an investigational treatment in patients, under the supervision of physicians and in accordance with strict ethical standards. Participation in a clinical trial is always voluntary and occurs only after patients receive complete and clear information. 

Discovery & Preclinical Research

Scientists start by identifying a promising molecule.

Lab tests and preclinical studies help understand how it works and if it's safe to move forward.

Phase 1

Clinical Trial: Phase 1

To assess safety & dosage

Small group of healthy volunteers or patients

 

Clinical Trial Phase 2

Clinical Trial: Phase 2

To evaluate effectiveness & confirm safety

Larger group of patients

Clinical Trial Phase 3

Clinical Trial: Phase 3

To confirm effectiveness & monitor safety

Even larger group of patients

Review & Approval

Throughout all phases, regulatory agencies such as the FDA and Health Canada review study data to ensure that human trials are safe for the patients.

At the end of Phase 3, they decide whether to approve the drug or treatment for public use.

Ongoing Monitoring

Even after approval, regulatory agencies continue to monitor safety and effectiveness.

Patient safety always comes first.

 * This page provides patients and families general information about these conditions, as well as insights into our innovative therapies and the ways they are developed — presented in an informative and supportive manner, while never replacing personalized medical advice.