Evaluation of Safety, Efficacy and Pharmacodynamic Effect of Bertilimumab in Patients With Bullous Pemphigoid

Pemphigoid, Bullous Clinical Trial

Official title:

An Open-Label, Proof of Concept Study Designed to Evaluate the Safety, Efficacy and Pharmacodynamic Effect of Bertilimumab in Patients With Newly Diagnosed, Moderate to Extensive Bullous Pemphigoid

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02226146
• Other study ID #: Immune/BRT/BP-01
• Status: Completed
• Phase: Phase 2
• Start date: February 2016
• Est. completion date: April 2018

Study information

• Verified date: May 2018
• Source: Immune Pharmaceuticals
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is an open-label, proof-of-concept, single group study in adult patients with newly diagnosed, moderate to extensive BP.

The study will consist of three periods: a screening period of up to 2 weeks, an open-label treatment period lasting 4 weeks consisting of IV infusion of bertilimumab on Days 0 and 14 and 28, and a safety and efficacy follow-up period of approximately 13 weeks.

Patients will receive concomitant oral steroids during the treatment and follow-up period.

Description:

This is an open-label, proof-of-concept, single group study in adult patients with newly diagnosed, moderate to extensive BP.

The study will consist of three periods: a screening period of up to 2 weeks, an open-label treatment period lasting 4 weeks consisting of IV infusion of bertilimumab on Days 0 and 14 and Day 28, and a safety and efficacy follow-up period of approximately 13 weeks.

Patients will receive concomitant oral steroids during the treatment and follow-up period. They will start on 30 mg prednisone daily (or equivalent). The initial dose will be maintained for at least 1 week, commencing on Day 0, until blister formation has ceased, crusts and erosions have disappeared and reepithelialization of lesions has started. The corticosteroid dose will then be reduced to 20 mg daily for 5 to 14 days. According to clinical response, this will be followed by corticosteroid dose reduction in 5 mg steps every 5 to 14 days until a dose of 10 mg daily is reached and then corticosteroid dose reduction in 2.5 mg steps every 5 to 14 days until the end of the study.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 11
• Est. completion date: April 2018
• Est. primary completion date: April 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 60 Years and older

Eligibility

Inclusion Criteria:

1. Males or females, = 60 years of age.

2. Karnofsky performance status > 60%

3. Newly diagnosed, Bullous Pemphigoid per standard diagnostic criteria:

• Clinical presentation [2]

• Skin biopsy from a fresh blister showing subepidermal clefting and an inflammatory infiltrate consisting mainly of eosinophils

• Immunofluorescence (IF) studies performed on uninvolved skin collected approximately 1 cm away from a fresh blister showing linear deposition of IgG and/or C3 along the basement membrane zone.

4. Moderate to extensive Bullous Pemphigoid defined by the mean number of new bullae and urticarial plaques that have appeared over the course of 3 days as determined by the investigator or referring physician (moderate disease defined by > 1 and = 10 new bullae daily and = 5 urticarial plaques and extensive disease by >10 new bullae daily) [3].

5. Adequate cardiac, renal and hepatic function as determined by the Investigator and demonstrated by screening laboratory evaluations, vital sign measurement, ECG recording and physical examination results.

6. Females of childbearing potential must agree to use effective contraception consistently throughout the study (such as hormonal contraception or two forms of barrier contraception) and have a negative serum pregnancy test at screening and a negative urine pregnancy test per the schedule of visits. Women are considered post-menopausal and not of childbearing potential if they have had 12 months of amenorrhea or have had surgical bilateral oophorectomy (with or without hysterectomy) or tubal ligation at least six weeks previously.

7. Males must have had a vasectomy or have expressed that they have no interest in fertility in the future.

8. Fertile males must agree to use effective contraception consistently throughout the study and for a period of four months following the end of study drug administration.

9. Willing and able to adhere to the study visit schedule and other protocol requirements.

10. Willing and able to provide voluntary written informed consent or written informed consent from a legally authorized representative with assent from the patient.

Exclusion criteria:

1. Patients with severe medical or surgical conditions at screening or baseline including, but not limited to, severe dementia or mental impairment, severe stroke, severe cardiac insufficiency, severe arterial hypertension, severe or uncontrolled renal, hepatic, hematological, gastrointestinal, endocrine, pulmonary, cardiac, neurologic, cerebral, psychiatric, or any other severe acute or chronic medical condition that may increase the risk associated with study participation/treatment or may interfere with the interpretation of study results and, in the Investigator's opinion, would make the patient inappropriate for study entry.

2. Presence of any malignancy that has been under active treatment (e.g., radiotherapy or chemotherapy) within the 2 years prior to baseline or is anticipated to require treatment during the study period (including follow up) with the exception of patients with removal of uncomplicated basal cell carcinoma or cutaneous squamous cell carcinoma, who may take part in the study.

3. Congenital or acquired immunodeficiency (e.g., common variable immunodeficiency, organ transplantation).

4. Clinically significant vital sign measurements or ECG findings as determined by the Investigator.

5. Clinically significant abnormal laboratory test results, unless regarded by the Investigator as related to BP, including but not limited to:

• Hemoglobin level <10.0 g/dL

• White blood cell count < 3 x 103/µL

• Lymphocyte count < 0.5 x 103/µL

• Platelet count <100 x 103/µL or >1200 x 103/µL

• Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) >3 the upper limit of normal (ULN)

• Alkaline phosphatase >3 ULN

• Serum creatinine >2 ULN

6. Patients with mild, relapsed or refractory Bullous Pemphigoid. Mild disease defined by the mean number of new lesions that have appeared over the course of 3 days as determined by the investigator or referring physician, as follows: = 1 bulla or < 5 urticarial plaques.

7. Concomitant skin conditions preventing physical evaluation of Bullous Pemphigoid.

8. Active or recent history of clinically significant infection within 1 month of baseline.

9. Pregnant or breast-feeding, or planning to become pregnant during the study.

10. Participation in a clinical trial of an investigational (unapproved) product within 4 weeks of baseline.

11. Known hypersensitivity to bertilimumab or any of the drug excipients.

12. Use of prednisone or other systemic steroids (excluding inhaled or ocular use of steroids) within 4 weeks prior to baseline. (Concomitant oral corticosteroids administered as part of the study protocol, from Day 0 onward, are allowed). Use of class 1 and 2 topical steroids (such as clobetasol propionate cream, reference Appendix D for further guidance) within 4 weeks prior to baseline. (Use of other topical steroids is allowed throughout the study at the discretion of the investigator).

13. Treatment with immunosuppressants (e.g., azathioprine, methotrexate) within 4 weeks prior to baseline.

14. Treatment with biologics (e.g., etanercept, adalimumab, ustekinumab, infliximab, intravenous Ig) within 4 months of baseline. Patients who have received rituximab within 1 year of baseline will be excluded from study participation.

15. Treatment with macrolides or tetracyclines within 4 weeks prior to baseline.

16. Received a vaccine or other immunostimulator within 4 weeks prior to baseline. Subject has current clinical, radiographic or laboratory evidence of active mycobacterium tuberculosis (TB) infection or prior evidence of active TB that, in the opinion of the investigator, has not been adequately treated or controlled and that represents a reactivation risk. If in the investigator's opinion the patient is at risk for latent TB, the patient should be evaluated for active/latent TB as applicable (e.g. PPD, QFT, and/or chest x-ray).

18. Evidence of an active disease of hepatitis B (HBsAg positive or HBcAb positive) or hepatitis C (HCV ab positive), CMV (IgM positive) or human immunodeficiency virus (HIV) infection (HIV1/2 Ab positive 19. Active abuse of alcohol or drugs. 20. Any other condition, which in the opinion of the Investigator would place the patient at an unacceptable risk if participating in the study protocol.

Related Conditions & MeSH terms

• Pemphigoid, Bullous

Intervention

Biological:
• Bertilimumab

Locations

Country	Name	City	State
Israel	Chaim Sheba MC, Tel-Hashomer	Ramat Gan
Israel	Sourasky-Ichilov Tel Aviv Medical Center	Tel Aviv
United States	University at Buffalo	Buffalo	New York
United States	University of Cleveland	Cleveland	Ohio
United States	Duke University Medical Center	Durham	North Carolina
United States	University of Iowa	Iowa City	Iowa
United States	Icahn School of Medicine at Mount Sinai	New York	New York
United States	University of Utah	Salt Lake City	Utah

Sponsors (1)

Lead Sponsor	Collaborator
Immune Pharmaceuticals

Countries where clinical trial is conducted

United States,  Israel, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Pharmacokinetic (PK) Endpoints - Cmax	• PK analysis for bertilimumab concentration: blood samples will be collected on dosing days (pre-dose, and at 30 minutes and 4 hours following initiation of study drug infusion) and once at remaining study visits (excluding screening). The following PK parameters will be calculated, to the degree possible given the number of timepoints: Cmax, Tmax, AUC, Vdist and t1/2. Additional standard and exploratory PK parameters will be calculated if deemed necessary. Cmax is the maximum bertilimumab serum concentration observed.	Participants will be followed the duration of the study, an expected average of 84 days
Other	Pharmacokinetic (PK) Endpoints - Tmax	• Tmax is the time until Cmax	Participants will be followed the duration of the study, an expected average of 84 days
Other	Pharmacokinetic (PK) Endpoints - AUC	• AUC is the area under the curve	Participants will be followed the duration of the study, an expected average of 84 days
Other	Pharmacokinetic (PK) Endpoints - Vdist	• Vdist is the volume of ditribution	Participants will be followed the duration of the study, an expected average of 84 days
Other	Pharmacokinetic (PK) Endpoints - T1/2	• T1/2 is the elimination half life	Participants will be followed the duration of the study, an expected average of 84 days
Other	Pharmacodynamic Endpoint: Change in autoantibody titres	• Change in BP180 and BP230 autoantibody titres at each scheduled sampling timepoint compared to baseline	Participants will be followed the duration of the study, an expected average of 84 days
Other	Pharmacodynamic Endpoint: Change in blood eosinophil count	• Change in blood eosinophil count at each scheduled sampling timepoint compared to baseline	Participants will be followed the duration of the study, an expected average of 84 days
Other	Pharmacodynamic Endpoint: Change in tissue eosinophil count	• Change in tissue eosinophil count assessed on biopsy at the scheduled timepoint compared to screening	Participants will be followed the duration of the study, an expected average of 84 days
Other	Pharmacodynamic Endpoint: Change in serum eotaxin-1 level	• Change in serum eotaxin-1 level at each scheduled sampling timepoint compared to baseline	Participants will be followed the duration of the study, an expected average of 84 days
Other	Exploratory Endpoint: Change in biomarkers	Change in PBMC biomarkers at each scheduled timepoint compared to baseline, including but not limited to: CD4, CD25, CD8, CD69, CD62L, CCR3 and Foxp3 via flow cytometry analyses.; Change in Eosinophil Cationic Protein serum levels	Participants will be followed the duration of the study, an expected average of 84 days
Primary	Safety Endpoints	Safety outcome would be assessed as the number of the following events which the participants experienced throughout the study: Number if Adverse events (AE); Injection site reactions after infusions; Abnormal Physical findings during the examination; Abnormal Vital signs (blood pressure, heart rate, temperature); Abnormal ECG; Number of Concomitant medications taken; Abnormal Laboratory values; Development of anti-bertilimumab antibodies	Participants will be followed for the duration of the study , an expected average of 118 days
Secondary	Efficacy Endpoint: Change in Bullous Pemphigoid Disease Area Index (BPDAI)	The BPDAI is a validated measure of bullous pemphigoid disease activity consisting of four subscores: skin blistering (0-120), uricaria (0-120), mucosal blistering (0-120) and damage/pigmentation (0-12). The activity score consists of the first three subscored (0-360); • Change in BPDAI Activity Score at each scheduled measurement timepoint	Participants will be followed for the duration of the study, an expected average of 84 days
Secondary	Efficacy Endpoint: BPDAI responders	• Proportion of subjects who achieve a reduction in BPDAI Activity Score of at least 50%, 75% and 90% at Days 42, 56, 70 or 84	Participants will be followed for the duration of the study, an expected average of 84 days
Secondary	Efficacy Endpoint: Prednisone dose	• Proportion of subjects who have tapered to prednisone dose of =10 mg/day at at Days 42, 56, 70 or 84	Participants will be followed for the duration of the study, an expected average of 84 days
Secondary	Efficacy Endpoint: Change in BPDAI pruritus component	• Change in pruritus visual analog scale (the sum of three 0-10 pruritus assessments: pruritus intensity over the prior day, week and month) at each scheduled measurement timepoint	Participants will be followed for the duration of the study, an expected average of 84 days
Secondary	Efficacy Endpoint: Change in Autoimmune Bullous Disease Quality of Life (ABQOL)	The ABQOL questionnaire is a validated 17 item questionnaire (range 0-51) assessing quality of life in patients with autoimmune blistering diseases; • ABQOL assessed at each scheduled measurement timepoint	Participants will be followed for the duration of the study, an expected average of 84 days
Secondary	Efficacy Endpoint: Control of disease activity	Control of disease activity is defined as the time when at least two of the following occur: new lesions cease to form, established lesions begin to heal and/or pruritic symptoms start to abate.; • Mean time from baseline to control of disease activity	Participants will be followed for the duration of the study, an expected average of 84 days