A Study to Evaluate Safety of Multi-Dose MEDI-545 in Adult Patients With Dermatomyositis or Polymyositis

• Register: ClinicalTrials.gov
• Last refreshed on: 19 February 2015
• Main ID: NCT00533091
• Date of registration: 20/09/2007
• Prospective Registration: Yes
• Primary sponsor: MedImmune LLC
• Public title: A Study to Evaluate Safety of Multi-Dose MEDI-545 in Adult Patients With Dermatomyositis or Polymyositis
• Scientific title: A Phase 1B, Randomized, Double-blind, Placebo-Controlled, Multicenter Study to Evaluate Safety of Multiple-Dose, Intravenously Administered MEDI-545, A Fully Human Anti Interferon-Alpha Monoclonal Antibody, In Adult Patients With Dermatomyositis or Polymyositis
• Date of first enrolment: April 2008
• Target sample size: 51
• Recruitment status: Completed
• URL: http://clinicaltrials.gov/show/NCT00533091
• Study type: Interventional
• Study design: Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
• Phase: Phase 1

Countries of recruitment

United States

Contacts

• Name: Dominique Ethgen, M.D.
• Affiliation: MedImmune LLC

Key inclusion & exclusion criteria

Inclusion Criteria:

- Male or female adults at least 18 years of age at the time of randomization;

- Written informed consent obtained from the patient or the patient's legal
representative prior to receipt of any study medication or beginning study
procedures;

- Probable or definite PM or DM according to the Bohan and Peter criteria (Bohan,
1975);

- For patients with PM, documentation of a muscle biopsy result that is consistent with
the diagnosis of PM;

- All patients including those with DM must meet at least two of the following
criteria:

- Strength in MMT greater = 80/150 but = 125/150 using the MMT-8 muscle group testing;

- Patient Global Activity Assessment by visual analog scale (VAS)= 2.0 cm on a 10 cm
scale, which is included as part of CLINHAQ;

- Physician Global Activity Assessment by VAS = 2.0 cm on a 10 cm scale, which is
included as part of MDAAT;

- CLINHAQ disability index = 0.25;

- Global extramuscular activity assessment = 1.0 cm on a 10-cm VAS scale (this measure
is the physician's composite evaluation and is based on assessments of activity
scores on the constitutional, cutaneous, skeletal, gastrointestinal, pulmonary and
cardiovascular scales of the MDAAT;

- Subjects with PM must have an elevation of serum CK or aldolase at a minimum level of
1.3 x upper limit of normal (ULN) or serum CK or aldolase at least 2-fold higher than
the patient's own lowest value since diagnosis;

- Subjects with DM must have either an elevated CK or aldolase as above (per inclusion
criterion #6) or other laboratory evidence of active myositis. This could include
either abnormal signal on skeletal muscle MRI suggestive of inflammation or an
electromyogram demonstrated muscle membrane irritability (e.g., fibrillation
potentials, positive sharp waves, complex repetitive discharges) and short duration,
small amplitude, polyphasic motor unit action potentials;

- For patients randomized to Dose Cohorts 1.2, 3A and 4: median fold overexpression of
the top 25 type I IFN inducible genes of four-fold or greater in whole blood at the
time of screening; For patients randomized to dose cohort 3B: low or negative
expression of type I IFN-inducible genes;

- Sexually active women, unless surgically sterile (including tubal ligation) or at
least 2 years postmenopausal, must use an effective method of avoiding pregnancy
(including oral, injectable, transdermal, or implanted contraceptives, intrauterine
device, diaphragm with spermicide, cervical cap, abstinence, and sterile sexual
partner) in addition to the use of condoms (male or female condoms with spermicide)
from screening through end of study. Cessation of birth control after this point
should be discussed with a responsible physician. Sexually active males, unless
surgically sterile, must likewise practice two effective methods of birth control
(condom with spermicide or abstinence) and must use such precautions from Study Day 0
through end of study;

- Ability to complete the study period, including follow-up period, of up to 350 days;
and

- Willing to forego other forms of experimental treatment during the study.

Exclusion Criteria:

- Receipt of MEDI-545 in any previous clinical study or prior randomization into the
trial;

- History of allergy or reaction to any component of the study drug formulation;

- Inclusion body myositis, cancer-associated myositis, myositis associated with another
connective tissue disease, environmentally-associated myositis, or drug-related
myopathy;

- A history of or a family history of noninflammatory myopathy, scapular winging,
atrophy, or hypertrophy of the calf muscles;

- Receiving prednisone > 35 mg/day (or an equivalent dose of another corticosteroid)
within 14 days before Study Day 0;

- Receiving the following dosages of medications within 28 days before Study Day 0:
hydroxychloroquine > 600 mg/day, mycophenolate mofetil > 3 g/day, methotrexate > 25
mg/week, azathioprine > 3 mg/kg/day, or any dose of cyclophosphamide, cyclosporine,
or thalidomide;

- Have received fluctuating doses of antimalarials, mycophenolate mofetil,
methotrexate, leflunomide, or azathioprine within 28 days before Study Day 0 or
fluctuating doses of corticosteroids within 14 days before Study Day 0;

- Have received leflunomide > 20 mg/day in the 6 months prior to Study Day 0;

- Treatment with any investigational drug therapy within 28 days before Study Day 0 or
biologic therapies (eg, rituximab) within 30 days or 5 half-lives of the biologic
agent, whichever is longer, before Study Day 0;

- In the investigator's opinion, evidence of clinically significant active infection,
including ongoing, chronic infection, within 28 days before Study Day 0;

- A history of severe viral infection as judged by the investigators, including severe
infections of either CMV or the herpes family such as disseminated herpes, herpes
encephalitis, ophthalmic herpes;

- Herpes zoster = 3 months prior to Study Day 0;

- Evidence of infection with hepatitis B or C virus or HIV-1 or HIV-2, or active
infection with hepatitis A, as determined by results of testing at screening;

- Vaccination with live attenuated viruses within 28 days before Study Day 0;

- Pregnancy (sexually active women, unless surgically sterile or at least 2 years
post-menopausal, must have a negative serum pregnancy test at screening and a
negative urine pregnancy test prior to study drug administration on Study Day 0);

- Breastfeeding or lactating women;

- History of alcohol or drug abuse < 1 year prior to Study Day 0;

- History of cancer, except for basal cell carcinoma or carcinoma in situ of the cervix
treated with apparent success with curative therapy more than 1 year prior to Study
Day 0;

- History of active tuberculous infection;

- History of latent tuberculous infection or newly positive TB skin test (reaction
defined as = 10 mm in diameter if not on systemic immunosuppressive medication or = 5
mm if on systemic immunosuppressive medication) without completion of an appropriate
course of treatment or ongoing prophylactic therapy;

- A history of coagulation disorders that in the opinion of the investigator would
contraindicate skin or muscle biopsies;

- Elective surgery planned from the time of screening through Study Day 196;

- At screening blood tests (must


Age minimum: 18 Years
Age maximum: N/A
Gender: Both

Health Condition(s) or Problem(s) studied

DERMATOMYOSITIS OR POLYMYOSITIS

Intervention(s)

Other: Placebo

Biological: MEDI-545

Primary Outcome(s)

The primary endpoints of the study are safety and tolerability of multiple intravenous (IV) doses of MEDI-545 in adult patients with Dermatomyositis or Polymyositis, assessed primarily by summarizing AEs assessing changes in viral cultures and titers. [Time Frame: 12 months]

Secondary Outcome(s)

The secondary endpoints of the study are the PK and IM of multiple IV doses of MEDI-545. [Time Frame: 12 months]

The third endpoint of the study are the evaluations of disease activities. [Time Frame: 12 months]

Secondary ID(s)

MI-CP151

Source(s) of Monetary Support

Please refer to primary and secondary sponsors