Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.
Inclusion Criteria:
1. Ability to understand the requirements of the trial, to provide written informed
consent (including consent for the use and disclosure of research-related health
information), willingness and ability to comply with the trial protocol procedures
(including required trial visits).
2. The participant is male or female, and aged from 18 years at the time of signing the
informed consent form (ICF).
3. The participant has a clinical diagnosis of PV (mucosal, cutaneous, mucocutaneous) or
PF which has been confirmed by cutaneous histology, positive direct immunofluorescence
(IF), and positive indirect IF and/or enzyme-linked immunosorbent assay (ELISA).
4. The participant meets one of the following profiles:
1. Newly diagnosed disease with PDAI ≥15 at baseline and naïve to treatment
2. Newly diagnosed disease with PDAI ≥15 while receiving a first course of oral
prednisone (or equivalent). According to clinical judgment, the participant has
shown no significant improvement of PV or PF signs for at least 2 weeks before
baseline and is considered fit to start prednisone treatment at 0.5 mg/kg qd at
baseline.
3. Experiencing flare with PDAI ≥15, a maximum of 4 years since diagnosis, and off
prednisone therapy ± a conventional immunosuppressant (e.g., azathioprine,
cyclophosphamide, methotrexate, mycophenolate mofetil) or dapsone. Note:
conventional immunosuppressants and dapsone must be discontinued before baseline.
4. Experiencing flare with PDAI ≥15, a maximum of 4 years since diagnosis, and
receiving a tapered dose of oral prednisone (or the equivalent), provided that
prednisone has been given at stable dose ± a conventional immunosuppressant for
at least 2 weeks and patients are fit to start prednisone treatment at 0.5 mg/kg
qd at baseline.
5. Contraceptive use by men and women should be consistent with local regulations
regarding the methods of contraception for those participating clinical trials and:
1. Male participants: Male participants must agree to use acceptable method of
contraception, and not donate sperm from signing the ICF until the end of the
study.
2. Female participants: Women of childbearing potential must:
- have a negative serum pregnancy test at screening and negative urine
pregnancy test at baseline before the IMP can be administered.
- agree to use a highly effective or acceptable contraception method, which
should be maintained at minimum until after the last dose of IMP
6. For Japanese participants enrolled in sites in Japan only: A Japanese participant is
defined as a participant whose parents and 4 grandparents are Japanese, and who has
Japanese nationality, was born in Japan, has not lived outside of Japan for a total of
>10 years, and currently lives in Japan.
Exclusion Criteria:
1. Participant has a confirmed diagnosis of paraneoplastic pemphigus, drug-induced
pemphigus, pemphigus vegetans, pemphigus erythematosus, or any other non-PV/non-PF
autoimmune blistering disease.
2. Participants with mild disease severity as defined by PDAI <15 at baseline.
3. Participants who show a significant improvement of PV or PF in the period from
screening to baseline according to clinical judgment (eg, the patient has achieved DC
or a substantial reduction in PDAI activity score during screening period).
4. The participant has been administered therapy(ies) other than oral prednisone or
conventional immunosuppressants (e.g., azathioprine, cyclophosphamide, methotrexate,
mycophenolate mofetil) or dapsone within 2 months before the baseline visit and that
can affect clinical disease activity. For example, excluded medications are
intravenous methylprednisolone, dapsone, sulfasalazine, tetracyclines, nicotinamide at
doses above the recommended daily allowance (RDA)/dietary reference intake (DRI),
plasmapheresis/ plasma exchange, immunoadsorption, and IVIg.
5. Use of any monoclonal antibody (including rituximab or another anti-CD20 biologic)
within 6 months before the baseline visit.
6. Known hypersensitivity to any of the components of the administered treatments.
7. The participant has a known contraindication to oral prednisone.
8. The participant has a history of refractory disease, as defined by a failure to
respond to first-line and second-line therapies
9. Participants who have a history of malignancy unless deemed cured by adequate
treatment with no evidence of recurrence for ≥3 years before first IMP administration.
Participants with any of the following cancers can be included at any time, provided
they are adequately treated prior to their participation in the study:
- Basal cell or squamous cell skin cancer,
- Carcinoma in situ of the cervix,
- Carcinoma in situ of the breast,
- Incidental histological finding of prostate cancer
10. Participants with clinical evidence of other significant serious disease or
participants who recently underwent or have planned a major surgery during the period
of the trial, or any other condition in the opinion of the investigator, that could
confound the results of the trial or put the patient at undue risk.
11. Pregnant and lactating women and those intending to become pregnant during the trial.
12. Current or history (i.e. within 12 months of screening) of alcohol, drug, or
medication abuse.
13. Any other known autoimmune disease that, in the opinion of the investigator, would
interfere with an accurate assessment of clinical symptoms of PV or PF or put the
participant at undue risk.
14. The participant has a Karnofsky Performance score <60%.
15. Vaccination with live viral vaccines within 28 days prior to randomization.
16. The participant has clinically significant uncontrolled active or chronic bacterial,
viral, or fungal infection.
17. Positive serum test at screening for an active viral infection with any of the
following conditions: Hepatitis B Virus, Hepatitis C Virus , HIV.
18. The participant has total immunoglobulin G (IgG) <6 g/L at screening.
19. The participant has previously participated in a trial with efgartigimod and has
received at least one administration of IMP.
20. Use of an investigational drug within 3 months or 5 half-lives of the drug (whichever
is longer) prior to first IMP administration
Note: Other protocol defined Inclusion/Exclusion criteria may apply.
Eligibility last updated 4/25/23. Questions regarding updates should be directed to the study team contact.