Efficacy, Safety and Pharmacokinetics of SPK-843 in the Treatment of Pulmonary Mycosis

NCT ID: NCT01125644

Last Updated: 2011-06-08

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE3
• Total Enrollment: 10 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-05-31
• Study Completion Date: 2011-12-31

Brief Summary

Recruitment of at least 10 adult patients (men and women) among individuals affected and admitted to the hospitals identified for the clinical study. All patients shall be between 18 and 75 years of age, with confirmed diagnosis of cryptococcosis or aspergillosis . During therapy (14 days) and examination (28 days), the patients will be subject to 7 doctor's visits (day 1,3,7,10,14,21, and 28).

Detailed Description

Objective: primary objective Evaluation of the overall global clinical response based on secondary end points from 1 to 6 at the end of the therapy (Study day 14) and at the final visit at the end of the study - follow-up- (Study day 28) in comparison to the initial clinical state.

The evaluation will be based on: improvement/normalization in relation to the semi-quantitative scales at 3, 4 and 5 items or at opinion expressed as positive for at least 3 of the first 6 secondary end points.

secondary objectives

1. Improvement on the basis of clinical symptoms;

2. Antifungal efficacy from the cultures;

3. Improvement on the basis of mycological blood testing;

4. Improvement on the basis of laboratory diagnosis (hemogasanalysis, ESR, CPR);

5. Improvement on the basis of radiological imaging (Rx, CAT HR,…);

6. Improvement on the basis of endoscopic examination;

7. Evaluate the plasma levels of SPK-843 after single dose and after multiple doses;

8. Evaluate the safety in the administration of SPK-843.

Methodology: Open label multi center study

Conditions

Cryptococcosis or Aspergillosis Infections

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Single Arm

Patients are males and females between 18 and 75 years of age with proven fungal etiology confirmed by mycological culture test and by hystopathological exam ("patients with definite diagnosis"), or patients with fungal infection of which is difficult to determine the etiological agent but with diagnosis of deep mycosis based on blood testing for fungal infection and/or clinical radiological examination, and/or endoscopic clinical examination, clinical symptomatology ("patients with clinical diagnosis").

Group Type: EXPERIMENTAL

SPK-843

Intervention Type: DRUG

SPK-843 is a semi-synthetic substance derived from Partricin A. 05 mg/Kg solution of SPK-843 in 10% intralipid will be administered i.v. in a hour for a treatment of 14 days

Interventions

SPK-843

SPK-843 is a semi-synthetic substance derived from Partricin A. 05 mg/Kg solution of SPK-843 in 10% intralipid will be administered i.v. in a hour for a treatment of 14 days

Intervention Type: DRUG

Other Intervention Names

SPA-S-843

Eligibility Criteria

Inclusion Criteria

• Patients with proven fungal etiology confirmed by mycological culture test and by hystopathological exam ("patients with definite diagnosis"), or patients with fungal infection of which is difficult to determine the etiological agent but with diagnosis of deep mycosis based on blood testing for fungal infection and/or clinical radiological examination, and/or endoscopic clinical examination, clinical symptomatology ("patients with clinical diagnosis").
• Patients being treated with other anti-fungal drugs (i) showing a poor response to the treatment at least after 5 days of administration of the anti-fungal drug, (ii) that have had an adverse reaction to the drug prejudicing its use, determining the risk/benefit ratio unfavorable to the patient.
• Patients between 18 and 75 years of age.
• Patients able to understand the content of the Informed Consent and willing to participate in the study.
• Male and female patients.
• Patients initially admitted to the hospitals identified for this clinical study.
• Informed Consent.

Exclusion Criteria

• Patients being treated with other anti-fungal drugs with improving clinical symptoms or with an unclear clinical course.
• Patients with intra-venous catheter and hospitalized with a diagnosis of fungemia but without clinical symptomatology twelve hours after the removal of the catheter.
• Patients with serious deep mycosis with low change of clinical efficacy (with a high probability of death event), or with serious concomitant illnesses or with complications, which may make difficult a safety evaluation of the treatment object of this study.
• Patients with a history of allergy to drugs like AMPH-B or with serious allergic reactions to drugs (shock after administration of drugs different from antifungals).
• Patients with serious hepatic, and/or renal, and/or cardiac failure or basic lung disease or with functionality of the organs with the following criteria:

• AST (GOT) or ALT (GPT) higher five (5) times the highest normal value or 200 UI/L;
• Blood creatinine higher than 2,0 mg/dl;
• Proteinuira (qualitative test) 3+ or greater, or a total urinary excretion of proteins (quantitative test) of 3,5 g/day or higher;
• Hyperkalemia or hypokalemia or with a basic level of sodium of 6,0 mEq/L or greater or less than 2,5 mEq/L;
• Hyperlipidemia with a basic value of total cholesterol greater than 1,5 times the highest normal values or 300 mg/dl, triglycerides higher than twice the highest normal values or 300 mg/dl;
• Patients that require the infusion of leucocytes;
• Patients with arterial thrombosis or with serious coagulative dysfunctions;
• Patients with diabetes mellitus associated with ketosis ;
• Pregnant women or women who intend to become pregnant, women in purperium, or breast feeding;
• Patients that participated in a clinical study (with any type of drugs, including anti-cancer drugs) or that have been recruited for observational clinical studies with pharmaceutical agents a month before the beginning of the treatment with SPK-843;
• Patients who, according to the doctor, are not considered fit to be recruited in the study.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Proaparts srl

INDUSTRY

Sponsor Role: lead

Responsible Party

Proaparts srl

Principal Investigators

Luigi Allegra, Ph.D.

Role: STUDY_DIRECTOR

Ospedale Maggiore di Milano IRCCS Policlinico

Francesco Blasi, MD

Role: PRINCIPAL_INVESTIGATOR

Ospedale Maggiore di Milano IRCCS Policlinico

Locations

Ospedale Maggiore di Milano IRCCS Policlinico Dipartimento Malattie Cardiovascolari e Respiratorie

Milan, , Italy

Site Status: RECRUITING

Countries

Italy

Central Contacts

Luigi Allegra, Ph.D

Role: CONTACT

luigi.allegra@unimi.it

39 02 55033781

Adolfo Gasparetto, Dr.

Role: CONTACT

adolfogasparetto@nextrasearch.it

39 0429 652545

Facility Contacts

Luigi Allegra, Ph.D

Role: primary

luigi.allegra@unimi.it

39 02 55033781

Other Identifiers

SPK-843-03/01

Identifier Type: -

Identifier Source: org_study_id