Safety of Photodynamic Therapy (PDT) in the Ablation of High-grade Dysplasia (HGD) in Barrett's Esophagus (BE) (Oedisse)

Pinnacle Biologics

Status and phase

Withdrawn

Phase 3

Conditions

Barrett Esophagus

Treatments

Procedure: Tissue sample collection

Procedure: Endoscopy with biopsy

Procedure: Electrocardiogram

Procedure: Blood collection

Procedure: Chest x-ray

Procedure: Endoscopy

Device: Medlight PDT Balloon

Study type

Interventional

Funder types

Industry

Identifiers

NCT01209013

MA-PO-PHOEST07-01

Details and patient eligibility

About

Photodynamic therapy (PDT) uses a combination of a drug, porfimer sodium, and a light from a non heated laser. The activation of the drug is done by lighting of abnormal areas using a fiber optic device. The fiber optic device is a very fine fiber (like a fishing line) that permits transmission of light. The fiber optic device is inserted into a diffusing balloon device to ensure the good positioning of the fiber optic within the esophagus (food pipe). It is thought that the size and the flexibility of a new diffusing balloon device could improve the safety profile of the photodynamic treatment by reducing the risk of narrowing or closure of the food pipe (esophageal stenosis) sometimes occurring after treatment.

This research study will evaluate the safety and effectiveness of PDT with porfimer sodium using a new diffusing balloon device for light application in the removal of high-grade dysplasia (HGD, precancerous change in the food pipe tissue) in Barrett's esophagus (BE). This study will provide advanced knowledge about phototoxicity (reaction similar to sunburn) and esophageal stenosis, main risks with this therapy. It will involve 75 patients with HGD in BE across North America and Europe and will last between 13 and 16 weeks. In addition, concentrations of porfimer sodium in the esophageal tissue will be analyzed in a subgroup of patients.

Full description

Patients with biopsy-confirmed HGD in BE will be evaluated to confirm eligibility. Prior to enrollment, all inclusion and exclusion criteria will be verified. Medical procedures including demographic information, medical/surgical history, concurrent medical conditions, physical exam (including vital signs, body weight, height, and skin color), degree of difficulty in swallowing; electrocardiogram, chest X-ray, clinical laboratory testing, concomitant medication intake and other therapy uses will be collected.

All patients will receive one course of PDT consisting of an intravenous injection of 2.0 mg/kg of porfimer sodium over 3-5 minutes followed by one or two endoscopic laser light applications. The first laser light application will be performed within 40-50 hours using a new diffusing balloon catheter. The second laser light application (without a diffusing balloon catheter) will be performed within 96-120 hours on those areas showing an insufficient response to the first application. Follow-ups (Weeks 4 and 13) will include some or all of the following procedures: physical exam; vital signs evaluation; body weight; endoscopy; skin, degree of difficulty in swallowing and esophageal stenosis assessment; and clinical laboratory check. All patients will be asked general open questions about any occurrence of adverse events, change in concurrent medical conditions, use of adjunctive therapy/procedure, and intake of concomitant medication. All patients will undergo rigorous systematic endoscopic biopsy surveillance at Week 13 (final visit).

Tissue concentration of oligomers (component of porfimer sodium) in normal and abnormal esophageal tissues will be determined in a subgroup of 12 patients. These patients will provide esophageal tissue samples before the porfimer sodium injection and on four separate occasions after the injection (22-26 hour-, 40-50 hour-, 96-120 hour-intervals, and 13 weeks).

All patients will be followed for three months.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients are males or females aged 18 or older.
Patients have been diagnosed with biopsy-proven HGD in BE.
Non-menopausal or non-surgically sterilized female patients must have a negative serum beta-HCG at the time of entry into the study.
Non-menopausal or non-surgically sterilized female patients must use a medically acceptable form of birth control.
Patients must sign an Informed Consent Form, which must comply with the ICH guidelines and local requirements.

Exclusion criteria

Patients who have previously received PDT for HGD in BE.
Patients who have previously undergone radiation therapy to the chest.
Patients with known porphyria or known hypersensitivity to porphyrins or any excipients of the porfimer sodium.
Patients who have esophageal cancer or in whom esophageal cancer, lymph node involvement, or metastases cannot be ruled out based on the pathology report, endoscopic ultrasonography (EUS), computed tomography (CT) scan or other diagnostic methods used in current practice no more than 30 days prior to date of consent.
Patients with any acute or chronic medical or psychological illnesses as judged clinically significant by the investigator to preclude PDT procedure.
Patients with a presence or history of neoplasms (treated during the last five years prior to study entry) other than carcinoma in situ of the cervix or basal carcinoma of the skin.
Patients with esophageal strictures, esophageal diverticula, esophageal or gastric varices.
Patients with known contraindications to analgesia or endoscopy.
Patients with blood parameters of Grade 3 or higher on the Common Terminology Criteria for Adverse Events (CTCAE).
Patients with unstable cardiovascular disease (Class III and IV cardiovascular disease according to the New York Heart Association's functional criteria).
Patients with esophageal ulcers > 1 cm in diameter.
Patients with tracheoesophageal or bronchoesophageal fistula.
Patients with chronic/acute dermatologic conditions (e.g., urticaria, eczema, sunburn).
Patients under anticoagulant therapy (only for the subgroup of 12 patients who will consent to provide tissue samples in order to determine the concentrations of oligomers).
Patients with severe renal or hepatic impairment with parameters of Grade 3 or higher on the CTCAE.
Patients who have been treated with any investigational drug during 60 days prior to the screening visit.
Patients who are unable or unwilling to complete the follow-up evaluations required for the study.