The VOLTAIRE-X Trial Looks at the Effect of Switching Between Humira® and BI 695501 in Patients With Plaque Psoriasis.

Inclusion criteria

- Males and females aged ≥ 18 to < 80 years at screening who have a diagnosis of
moderate-to-severe chronic plaque psoriasis (with or without psoriatic arthritis) for
at least 6 months before the first administration of trial drug (a self-reported
diagnosis confirmed by the Investigator is acceptable), and which has been stable per
Investigator opinion for the last 2 months with no changes in morphology or
significant flares at both screening and baseline:

- involved body surface area (BSA) ≥ 10% and

- PASI score ≥ 12 and

- sPGA score of ≥ 3.

- Participants of reproductive potential (childbearing potential1) must be willing and
able to use highly effective methods of birth control per International Council for
Harmonisation (ICH) M3 (R2) that result in a low failure rate of less than 1% per year
when used consistently and correctly during the trial and for 6 months following
completion or discontinuation from the trial medication. A list of contraception
methods meeting these criteria is provided in patient information.

- Signed and dated written informed consent in accordance with Good Clinical Practice
(GCP) and local legislation prior to admission to the trial.

- Patients who are candidates for systemic therapy or phototherapy according to
Investigator judgement.

Exclusion criteria

- Active ongoing inflammatory diseases other than psoriasis that might confound trial
evaluations according to Investigator's judgment.

- Prior exposure to any biologic therapies for any auto-immune diseases (eg: RA,
Psoriasis, Crohns Disease, etc).

- Patients with a significant disease other than psoriasis and/or a significant
uncontrolled disease (such as, but not limited to, nervous system, renal, hepatic,
endocrine, hematological, autoimmune or gastrointestinal disorders). A significant
disease is defined as a disease which, in the opinion of the Investigator, may (i) put
the patient at risk because of participation in the trial, or (ii) influence the
results of the trial, or (iii) cause concern regarding the patient's ability to
participate in the trial.

- Major surgery (major according to the Investigator's assessment) performed within 12
weeks before enrollment or planned within 6 months after screening, e.g., total hip
replacement.

- Any documented active or suspected malignancy or history of malignancy within 5 years
prior to screening, except appropriately treated (in the opinion of the Investigator)
basal cell carcinoma of the skin or in situ carcinoma of uterine cervix.

- Patients who must or wish to continue the intake of restricted medications or any drug
considered likely to interfere with the safe conduct of the trial.

- Currently enrolled in another investigational device or drug trial, or less than 30
days (or less than 5 half-lives, whichever is longer) since ending another
investigational device or drug trial(s), or receiving other investigational
treatment(s).

- Chronic alcohol or drug abuse or any condition that, in the Investigator's opinion,
makes the patient an unreliable trial subject or unlikely to complete the trial.

- Women who are pregnant, nursing, or who plan to become pregnant during the course of
this trial or within the period at least 6 months following completion or
discontinuation from the trial medication.

- Forms of psoriasis (e.g., pustular, erythrodermic and guttate) other than chronic
plaque psoriasis. Drug-induced psoriasis (i.e., new onset or current exacerbation from
e.g., beta blockers or lithium).

- Primary or secondary immunodeficiency (history of, or currently active), including
known history of HIV infection or a positive HIV test at screening (per the
Investigator discretion and where mandated by local authorities).

- Known chronic or relevant acute TB; IGRA TB test or PPD skin test will be performed
according to the labelling for Humira®. If the result is positive, patients may
participate in the trial if further work up (according to local practice/guidelines)
establishes conclusively that the patient has no evidence of active TB. If latent TB
is confirmed, then treatment must have been initiated before treatment in the study
and continued according to local country guidelines.

- Known clinically significant (per Investigator opinion) coronary artery disease,
significant cardiac arrhythmias, moderate to severe congestive heart failure (New York
Heart Association Classes III or IV) or interstitial lung disease observed on chest
X-ray.

- Patients with a history of any clinically significant adverse reaction (including
serious allergic reactions, or anaphylactic reaction, or hypersensitivity) to murine
or chimeric proteins, previously used biological drug or its excipients, or natural
rubber and latex.

- Positive serology for HBV or HCV.

- Receipt of a live/attenuated vaccine within 12 weeks prior to the Screening Visit;
patients who are expecting to receive any live/attenuated virus or bacterial
vaccinations during the trial or up to 3 months after the last dose of trial drug.

- Any treatment (including biologic therapies) that, in the opinion of the Investigator,
may place the patient at unacceptable risk during the trial.

- Known active infection of any kind (excluding fungal infections of nail beds), any
major episode of infection requiring hospitalisation or treatment with intravenous
(i.v.) antiinfectives within 4 weeks of the Screening Visit or completion of oral
anti-infectives within 2 weeks of the Screening Visit.

- Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) > 2.5 times upper
limit of normal (ULN) at screening.

- Hemoglobin < 8.0 g/dL at screening.

- Platelets < 100,000/μL at screening.

- Leukocyte count < 4000/μL at screening.

- Calculated creatinine clearance < 60 mL/min at screening.