Safety and Efficacy of Intramuscular Electrotransfer of Plasmid AMEP in Patients Suffering From Advanced or Metastatic Melanoma (AIMM)

Onxeo

Status and phase

Withdrawn

Phase 2

Phase 1

Conditions

Melanoma

Treatments

Biological: naked DNA coding for protein AMEP

Study type

Interventional

Funder types

Industry

Identifiers

NCT01764009

BA2011/15/02

2011-005538-20 (EudraCT Number)

Details and patient eligibility

About

The objective of the present trial is:

to determine the dose limiting toxicity (DLT), maximal tolerated dose (MTD) and recommended phase 2 dose (RP2D) of intramuscular electrotransferred Plasmid AMEP in patients with advanced or metastatic melanoma.
to determine the local and general safety of intramuscular electrotransferred Plasmid AMEP
to evaluate the efficacy of intramuscular electrotransferred Plasmid AMEP

Full description

In this open-label, multicentre, dose escalation phase I study, successive cohorts of 3 patients suffering from advanced or metastatic melanoma will be electrotransferred increasing doses of Plasmid AMEP into muscle. Treatment will be repeated every 28 days until progression or limiting toxicity.

Consecutive cohorts of 3 to 6 patients will be treated with increasing doses of Plasmid AMEP at three dose levels: 0.25 mg, 1 mg and 4 mg according to an adapted 3+3 design. There will be no intra-patient dose escalation.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Aged over 18 years
Patient with histologically or cytologically confirmed melanoma
Patient with unresectable advanced or metastatic (stage III or IV) melanoma
Patient with progressive melanoma (any BRAF status is permitted) not responding or intolerant to previous treatments, including patients with asymptomatic and not rapidly progressive brain metastases.
Patient with a minimum of one measurable lesion according to RECIST guideline 1.1
Eastern Cooperative Oncology Group (ECOG) performance status 0, 1 or 2
Patient having given a written informed consent

Exclusion criteria

Patient eligible for curative treatments and/or any palliative treatments with demonstrated efficacy, including current treatments for brain metastasis, and including available BRAF inhibitors as indicated for patients carrying B-RAF mutated tumours if applicable.
Patient with history of any other cancer within five years before enrollment (except cured basal cell carcinoma or cervical cancer in situ)
Patient with inadequate organ function, defined as:
Platelet count < 75.103 /L (> grade 2 NCI CTCAE)
Absolute neutrophil count < 1.109 /L (> grade 2)
Hemoglobin < 9 g/dL
INR increased or prolonged activated partial thromboplastin time (aPTT) upper the limit of normal (ULN) (≥ grade 1)
Creatinine clearance < 60 mL/min (Cockcroft and Gault formula) (≥ grade 2)
Patient with ALT > 3 ULN (≥ grade 2) or patient with symptomatic liver metastasis with ALT > 5 ULN (> grade 2)
Serum Total Bilirubin > 1.5 ULN (≥ grade 2); Patient with Gilbert's syndrome could be included if hyperbilirubinemia ≤ 3 ULN
Not medically controlled coagulation disorder (i.e hemophilia, protein C or S deficiency...)
Patient with electronic pacemakers, defibrillators, or any implanted electronic device
Any cardiac dysrhythmia (> grade 2) (i.e significant ventricular arrhythmia as persistent ventricular tachycardia and/or ventricular fibrillation; severe conduction disorders as atrio-ventricular block 2 and 3, sino-atrial block)
Recent (less than 6 months) acute vascular diseases (i.e stroke, myocardial infarction)
Arterial vascular disorders ≥ grade 2
Serious, non-healed wound, ulcer or bone fracture
Significant traumatic injury within 28 days prior to study treatment start or anticipation of the need for major surgery during study treatment
Evidence of ongoing or active viral or bacterial infection ( i.e bacterial infection requiring IV antibiotics)
Patient with life expectancy less than 3 months
Prior systemic therapy or any other antineoplastic treatments within the last 4 weeks, including radiotherapy or surgery
Patients who had participated in another clinical trial in the last 30 days prior to enrolment in the present clinical trial
Man and woman of child-bearing age without effective contraception method during the study and for 3 months after the last administration of Plasmid AMEP (i.e oral contraception or intra-uterine device for woman; i.e condom for man)
Pregnant or nursing women
Any significant disease, including psychiatric and neuromuscular disease, which may affect the proper evaluation of safety or efficacy or may affect ability to give informed consent
Patients unwilling or unable to comply with protocol requirements and scheduled visits
For contrast enhanced ultrasound (CEUS): known contraindications to SonoVue as described in the summary product characteristics (i.e cardiac or pulmonary history, hypersensitivity to sulphur hexafluoride or to any of the components of SonoVue)
For the part II: prophylactic phenytoin in combination with dacarbazine.