Ilumya

The solution is clear to slightly opalescent and colourless to slightly yellow. The solution pH is in the range of 5.7-6.3 and the osmolality is between 258 and 311 mOsm/kg.
Each pre-filled syringe contains 100 mg of tildrakizumab in 1 mL.
Tildrakizumab is a humanised IgG1/k monoclonal antibody produced in Chinese Hamster Ovary (CHO) cells by recombinant DNA technology.
Excipient with known effect: Each Tildrakizumab 100 mg solution for injection in pre-filled syringe contains 0.5 mg of polysorbate 80 (E 433).
Excipients/Inactive Ingredients: L-Histidine, L-Histidine hydrochloride monohydrate, Polysorbate 80 (E 433), Sucrose, Water for injections.

Pharmacotherapeutic group: Immunosuppressants, interleukin inhibitors. ATC code: L04AC17.
Pharmacology: Pharmacodynamics: Mechanism of action: Tildrakizumab is a humanised IgG1/k monoclonal antibody that specifically binds to the p19 protein subunit of the interleukin-23 (IL-23) cytokine without binding to IL-12 and inhibits its interaction with the IL-23 receptor.
IL-23 is a naturally occurring cytokine that is involved in inflammatory and immune responses. Tildrakizumab inhibits the release of proinflammatory cytokines and chemokines.
Clinical efficacy and safety: The multicentre, randomised, double-blind, placebo-controlled trials reSURFACE 1 and reSURFACE 2 studies enrolled a total of 1,862 patients 18 years of age and older with plaque psoriasis who had a minimum body surface area involvement of 10%, a Physician Global Assessment (PGA) score of ≥3 in the overall assessment (plaque thickness, erythema, and scaling) of psoriasis on a severity scale of 0 to 5, a Psoriasis Area and Severity Index (PASI) score ≥12, and who were candidates for phototherapy or systemic therapy.
In these studies, patients were randomised to either placebo or tildrakizumab (including 200 mg and 100 mg at 0, 4 and every twelve weeks thereafter [Q12W]), up to 52 or 64 weeks. In the active comparator study (reSURFACE 2), patients were also randomised to receive etanercept 50 mg twice weekly for 12 weeks, and weekly thereafter up to 28 weeks. Patients who did not respond to etanercept treatment (<75% reduction in PASI from baseline) were switched to tildrakizumab 200 mg Q12W up to 52 weeks, while patients who responded to etanercept were discontinued from the study.
Eligible patients who completed the double-blind periods of reSURFACE 1 and reSURFACE 2 with ≥50% improvement in PASI from baseline could participate in open-label extension phases of these studies in order to evaluate the long-term safety and maintenance of efficacy of continuous tildrakizumab treatment. Patients entering the extension periods of reSURFACE 1 and reSURFACE 2 continued treatment at the same dose of tildrakizumab, 100 mg or 200 mg, that they were receiving at week 64 or 52, respectively. Up to 6 years of follow-up data are available.
Overall demographic and baseline characteristics in reSURFACE 1 and reSURFACE 2 studies were consistent across individual trials. Patients were 18 to 82 years old, with a mean age of 45.9 years old. The median baseline PASI score ranged from 17.7 to 18.4 across treatment groups. Baseline PGA score was marked or severe in 33.4% of patients. Of all patients, 35.8% had received prior phototherapy, 41.1% had received prior conventional systemic therapy, 16.7% had received prior biologic therapy for the treatment of plaque psoriasis. A total of 15.4% of study patients had a history of psoriatic arthritis. Mean baseline Dermatology Life Quality Index (DLQI) ranged from 13.0 to 14.8.
Studies reSURFACE 1 and reSURFACE 2 assessed the changes from baseline at Week 12 in the two co-primary endpoints: 1) PASI 75 and 2) PGA of "0" (cleared) or "1" (minimal), with at least a 2-point improvement from baseline. Other evaluated outcomes included the proportion of patients who achieved PASI 90, PASI 100, the proportion of patients with DLQI 0 or 1, and maintenance of efficacy up to 52/64 weeks.
Results obtained at weeks 12, 28 and beyond (up to week 64 in reSURFACE 1 and up to week 52 in reSURFACE 2) are presented in Table 1 and Table 2. (See Table 1.)

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Maintenance of response: The maintenance of response in studies reSURFACE 1 and reSURFACE 2 is presented in Table 2. Maintenance and durability of PASI 90 response over time is presented in Figure 1. (See Table 2 and Figure 1.)

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Click on icon to see table/diagram/image

Of the patients who completed the double-blind period, 506 (79%) in reSURFACE 1 and 730 (97%) in reSURFACE 2 entered the extension period. Across studies, at least 76% of patients who had a PASI 90 response at the end of double-blind period, maintained a PASI 90 response during the extension period, when tildrakizumab 100 mg or 200 mg treatment was continued during a period of 192 weeks (Figure 2 and Figure 3). (See Figures 2 and 3.)

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Click on icon to see table/diagram/image

Quality of life/patient-reported outcomes: At week 12 and across studies, tildrakizumab was associated with statistically significant improvement in health-related quality of life as assessed by the DLQI (Table 2). Improvements were maintained over time with at week 52, 63.7% (100 mg) and 73.3% (200 mg) in reSURFACE 1, and 68.8% (100 mg) and 72.4% (200 mg) in reSURFACE 2 of patients who were PASI 75 responders at week 28 having a DLQI of 0 or 1.
Immunogenicity: In pooled Phase 2b and Phase 3 analyses, 7.3% of tildrakizumab-treated patients developed antibodies to tildrakizumab up to week 64. Of the subjects who developed antibodies to tildrakizumab, 38% (22/57 patients) had neutralizing antibodies. This represents 2.8% of all subjects receiving tildrakizumab.
In pooled phase 3 analyses, 8.3% of tildrakizumab-treated patients developed antibodies to tildrakizumab up to 420 weeks of treatment. Of the tildrakizumab-treated patients who developed antibodies to tildrakizumab, 35% (36/102 patients) had antibodies that were classified as neutralizing, which represents 2.9% of all tildrakizumab-treated patients.
The development of neutralizing antibodies to tildrakizumab was associated with lower serum tildrakizumab concentrations.
Paediatric population: The safety and efficacy of tildrakizumab in children and adolescents below the age of 18 years have not yet been established. No data are available.
Pharmacokinetics: Absorption: The subcutaneous formulation of tildrakizumab showed an absolute bioavailability ranging from 73% (90% CI: 46%-115%, 200 mg subcutaneous vs. 3 mg/kg intravenous) to 80% (90% CI: 62%-103%, 50 mg subcutaneous vs. 0.5 mg/kg intravenous) in healthy subjects, as a result of cross study single dose comparison. Maximum concentration was reached at 6.2 days after injection. Population pharmacokinetic analysis indicated a 31% higher bioavailability in healthy subjects compared to patients.
At steady state, following administration of 100 mg of tildrakizumab in subjects with moderate to severe plaque psoriasis geometric means (% coefficient of variation [%CV]) of AUC_0-τ and C_max values were respectively 305 μg·day/mL (41%) and 8.1 μg/mL (34%), whereas they were 612 μg·day/mL (40%) and 16.3 μg/mL (33%) following administration of 200 mg.
Distribution: Tildrakizumab has limited extravascular distribution with volume of distribution (Vd) values ranging from 76.9 to 106 mL/kg.
Biotransformation: Tildrakizumab is catabolised into component amino acids by general protein degradation processes. Small-molecule metabolic pathways (e.g., CYP450 enzymes, glucuronosyltransferases) do not contribute to its clearance.
Elimination: Clearance values range from 2.04 to 2.52 mL/day/kg and the half-life was 23.4 days (23% CV) in subjects with plaque psoriasis.
Linearity/non-linearity: Tildrakizumab exhibited dose-proportional pharmacokinetics in subjects with plaque psoriasis over a dose range from 50 mg to 400 mg following subcutaneous administration, with clearance being independent of dose.
Steady-state is achieved by 16 weeks with the clinical regimen of 0, 4, and every 12 weeks thereafter, with 1.1-fold accumulation in exposure between week-1 and week-12 independent of dose.
Pharmacokinetics in special populations: Elderly: Population pharmacokinetic analysis indicated that age did not have a clinically significant influence on the clearance of tildrakizumab in adult subjects with plaque psoriasis. Following administration of 100 mg or 200 mg of tildrakizumab, subjects who are 65 years or older (n=81 and n=82, respectively) had a similar tildrakizumab clearance as compared to subjects less than 65 years old (n=884).
Renal and hepatic impairment: No formal trial of the effect of hepatic or renal impairment on the pharmacokinetics of tildrakizumab was conducted. Tildrakizumab is catabolised into component amino acids by general protein degradation processes and is not eliminated by renal or hepatic pathways.
Body weight: Population pharmacokinetic modelling indicated that exposure decreased as body weight increased. The geometric mean exposure (AUC0-τ at steady state) in adult patients weighing >90 kg following a 100 mg or 200 mg subcutaneous dose was predicted to be about 30% lower than in an adult patient weighing ≤90 kg (see Dosage & Administration).
Drug interactions: Results from a drug-drug interaction study conducted in plaque psoriasis subjects suggest that tildrakizumab had no clinically relevant effect on CYP1A2, CYP2C9, CYP2C19, CYP2D6 and CYP3A4. Therefore, tildrakizumab does not impact the pharmacokinetics of concomitant medicinal products metabolised by CYP enzymes (see Interactions).
Toxicology: Preclinical safety data: Non-clinical data reveal no special hazard for humans based on conventional studies of safety pharmacology, and repeated dose toxicity.
Animal mutagenicity and carcinogenicity studies have not been conducted with tildrakizumab. Studies in mouse tumor models showed that selective inhibition of IL-23p19 does not increase carcinogenic risk.
In cynomolgus monkeys, there was negligible secretion of the product into breast milk. One month after birth, the milk/serum ratio was ≤0.002. Tildrakizumab was shown to distribute across the placental barrier. After repeated dosing to pregnant cynomolgus monkeys, serum concentrations were quantifiable in the fetus, but the reproduction toxicity studies did not reveal any untoward effects.
No effects on fertility parameters such as reproductive organs, menstrual cycle length, and/or hormones were observed in male and female cynomolgus monkeys that were administered tildrakizumab at doses resulting in >100 times the human exposure at the recommended clinical dose based on AUC.
In a pre- and postnatal development toxicity study in monkeys, no related increase in pregnancy loss was observed at exposures up to 85 times the human exposure at the recommended dose. No harmful effects were noted in neonates at maternal exposures up to 9 times the human exposure at the recommended dose. Two neonatal deaths from monkeys administered tildrakizumab at maternal exposure of 85 times the human exposure at the recommended dose were attributed to possible viral infection and considered of uncertain relationship to the treatment. The clinical significance of these findings is unknown.

ILUMYA (tildrakizumab) is indicated for the treatment of adults with moderate-to-severe plaque psoriasis who are candidates for systemic therapy or phototherapy.

This medicinal product is intended for use under the guidance and supervision of a physician experienced in the diagnosis and treatment of plaque psoriasis.
Posology: The recommended dose is 100 mg by subcutaneous injection at weeks 0, and 4 and every 12 weeks thereafter.
At the physician's discretion, in patients with high disease burden or in patients above 90 kg of body weight a dose of 200 mg may provide greater efficacy.
Consideration should be given to discontinuing treatment in patients who have shown no response after 28 weeks of treatment. Some patients with initial partial response may subsequently improve with continued treatment beyond 28 weeks.
Missed dose: If a dose is missed, the dose should be administered as soon as possible. Thereafter, dosing should be resumed at the regular scheduled time.
Special populations: Elderly: No dose adjustment is required (see Pharmacology: Pharmacokinetics under Actions).
Renal or hepatic impairment: Tildrakizumab has not been studied in these patient populations. No dose recommendations can be made. For further information on elimination of tildrakizumab, see Pharmacology: Pharmacokinetics under Actions.
Paediatric population: The safety and efficacy of tildrakizumab in children and adolescents below the age of 18 years have not yet been established. No data are available.
Method of administration: This medicinal product is administered by subcutaneous injection. Injection sites should be alternated. Tildrakizumab should not be injected into areas where the skin is affected by plaque psoriasis or is tender, bruised, red, hard, thick, or scaly. The syringe must not be shaken. Each syringe is for single use only.
After proper training in subcutaneous injection technique, patients may self-inject tildrakizumab if a physician determines that it is appropriate. However, the physician should ensure appropriate follow-up of patients. Patients should be instructed to inject the full amount of tildrakizumab according to the instructions provided in the package leaflet. Comprehensive instructions for administration are given in the medication guide.

Doses up to 10 mg/kg intravenously have been safely administered in clinical trials.
In the event of overdose, it is recommended that the patient be monitored for any signs or symptoms of adverse reactions and that appropriate symptomatic treatment be instituted immediately.

Hypersensitivity to the active substance or to any of the excipients.
Clinically important active infection, e.g. active tuberculosis (see Precautions).

Traceability: In order to improve the traceability of biological medicinal products, the name and the batch number of the administered product should be clearly recorded.
Infections: Tildrakizumab has the potential to increase the risk of infection (see Adverse Reactions).
Caution should be exercised when considering the use of tildrakizumab in patients with a chronic infection or a history of recurrent or recent serious infection.
Patients should be instructed to seek medical advice if signs or symptoms suggestive of a clinically relevant chronic or acute infection occur. If a patient develops a serious infection, the patient should be closely monitored and tildrakizumab should not be administered until the infection resolves (see Contraindications).
Pre-treatment evaluation for tuberculosis: Prior to initiating treatment, patients should be evaluated for tuberculosis (TB) infection. Patients receiving tildrakizumab should be closely monitored for signs and symptoms of active TB during and after treatment. Anti-TB therapy should be considered prior to initiating treatment in patients with a past history of latent or active TB in whom an adequate course of treatment cannot be confirmed.
Hypersensitivity: If a serious hypersensitivity reaction occurs, administration of tildrakizumab should be discontinued immediately and appropriate therapy initiated (see Contraindications).
Vaccinations: Prior to initiating treatment with tildrakizumab, consider completion of all appropriate immunisations according to current immunisation guidelines. If a patient has received live viral or bacterial vaccination it is recommended to wait at least 4 weeks prior to starting treatment with tildrakizumab. Patients treated with tildrakizumab should not receive live vaccines during treatment and for at least 17 weeks after treatment (see Interactions).
Excipients: This medicine contains 0.5 mg of polysorbate 80 (E 433) in each pre-filled syringe of 100 mg. Polysorbates may cause allergic reactions.
Effects on ability to drive and use machines: Tildrakizumab has no or negligible influence on the ability to drive and use machines.

Women of childbearing potential: Women of childbearing potential should use an effective method of contraception during treatment and for at least 17 weeks after treatment.
Pregnancy: There is no or limited amount of data (less than 300 pregnancy outcomes) from the use of tildrakizumab in pregnant women. Animal studies do not indicate direct or indirect harmful effect with respect to reproductive toxicity (see Pharmacology: Toxicology: Preclinical safety data under Actions). As a precautionary measure, it is preferable to avoid the use of tildrakizumab during pregnancy.
Breast-feeding: It is unknown whether tildrakizumab is excreted in human milk. Available toxicological data in cynomolgus monkey have shown negligible levels of tildrakizumab in milk on postnatal day 28 (see Pharmacology: Toxicology: Preclinical safety data under Actions). In humans, during the first few days after birth antibodies may be transferred to the newborns through milk. In this short period, a risk to the newborns/infants cannot be excluded. A decision must be made whether to discontinue breast-feeding or to discontinue/abstain from tildrakizumab therapy taking into account the benefit of breast-feeding for the child and the benefit of therapy for the woman.
Fertility: The effect of tildrakizumab on human fertility has not been evaluated. Animal studies do not indicate direct or indirect harmful effects with respect to fertility (see Pharmacology: Toxicology: Preclinical safety data under Actions).

Summary of the safety profile: The most common adverse reactions are upper respiratory tract infections (12.6%), headache (4.0%), diarrhoea (1.6%), gastroenteritis (1.5%), back pain (1.5%), nausea (1.3%) and injection site pain (1.3%).
Tabulated list of adverse reactions: Adverse reactions from clinical studies (Table 1) are listed by MedDRA system organ class (SOC) and frequency, using the following convention: very common (≥1/10); common (≥1/100 to <1/10); uncommon (≥1/1 000 to <1/100); rare (≥1/10 000 to <1/1 000); very rare (<1/10 000); and not known (cannot be estimated from available data). Within each frequency grouping, adverse reactions are presented in the order of decreasing seriousness. (See Table 3.)

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Long-term Safety: The safety profile of tildrakizumab observed during the long-term extensions periods of reSURFACE 1 and reSURFACE 2 was consistent with that of the double-blind periods.

Vaccines: No data are available on the response to live or inactivated vaccines. Live vaccines should not be given concurrently with tildrakizumab (see Precautions).
Interactions with cytochrome P450: Concomitant medicinal products affecting tildrakizumab pharmacokinetics are not expected since it is cleared from the body by general protein catabolism processes with no contribution of cytochrome P450 (CYP450) enzymes, and it is not eliminated by renal or hepatic pathways. Furthermore, tildrakizumab does not impact the pharmacokinetics of concomitant medicinal products metabolised by CYP450 enzymes either through direct or indirect mechanisms (see Pharmacology: Pharmacokinetics under Actions).
Interactions with other immunosuppressive agents or phototherapy: The safety and efficacy of tildrakizumab in combination with other immunosuppressive agents, including biologics, or phototherapy has not been evaluated.

Incompatibilities: In the absence of compatibility studies, this medicinal product must not be mixed with other medicinal products.
Special precautions for disposal and other handling: Tildrakizumab is a sterile solution for injection in pre-filled syringe. The syringes are for single use only.
Do not shake or freeze. The syringe should be taken out of the refrigerator 30 minutes before injecting to allow it to reach room temperature (up to 25°C).
Prior to use, a visual inspection of the syringe is recommended. A small air bubble may be apparent: this is normal. Do not use if the liquid contains easily visible particles, is cloudy or is distinctly brown.
The instructions for use included with the medication guide must be followed carefully.
Any unused medicinal product or waste material should be disposed of in accordance with local requirements.

Store refrigerated at 2°C to 8°C (36°F to 46°F) in the original carton to protect from light until the time of use. Tildrakizumab can be kept at 25°C (77°F) for up to 30 days or at 30°C (86°F) for up to 3 days in the original carton to protect from light. Once stored at 25°C or 30°C, do not place back in the refrigerator. If not used within 30 days at 25°C or within 3 days at 30°C, discard tildrakizumab. Do not freeze. Do not shake.
Shelf life: 3 years.

Instructions of Use: Before using the pre-filled syringes: Important points to know: Before you use ILUMYA pre-filled syringes, read and carefully follow all the step-by-step instructions. Keep the instructions for use and refer to them as needed.
The pre-filled syringes must not be shaken.
Preparation: 1. Take a pack from the refrigerator (if stored in the refrigerator): Take a carton pack out of the refrigerator and place the original and unopened carton pack on a clean and flat working surface.
2. Wait for 30 minutes (if stored in the refrigerator): Leave the pre-filled syringe in the ILUMYA carton (with the lid closed) and let it sit at room temperature for 30 minutes.
3. Inspect the medicine: Remove the pre-filled syringe from the carton when ready to inject. Check the expiration date on the carton and pre-filled syringe and discard if the date has passed.
DO NOT pull off the needle cover until you are ready to inject.
Inspect ILUMYA visually for particulate matter and discolouration prior to administration.
ILUMYA is a clear to slightly opalescent and colourless to slightly yellow solution.
DO NOT use if the liquid contains visible particles or the syringe is damaged. Air bubbles may be present; there is no need to remove them.
DO NOT use the product if it has been dropped on a hard surface or damaged.
4. Collect all the materials you need: On a clean, well-lit work surface, place the alcohol wipes, cotton ball or gauze pad, sticking plaster, sharps disposal container.
5. Wash your hands: Wash your hands thoroughly with soap and water.
6. Choose an injection site: Choose an injection site with clear skin and easy access such as abdomen, thighs or upper arm.
DO NOT administer 5 cm around the navel or where the skin is tender, bruised, abnormally red, hardened or affected by psoriasis.
DO NOT inject into scars, stretch marks, or blood vessels.
The upper arm is only suitable when someone else is injecting you.
7. Clean injection site: Clean the injection site with an alcohol wipe and allow the skin to dry.
Do not touch this area again before giving the injection.
8. Pull off the needle cover: While holding the body of the pre-filled syringe, remove the needle cover as shown and discard. You may see 1 or 2 drops of liquid and that is okay.
DO NOT touch the blue plunger yet.
DO NOT use if pre-filled syringe or needle is bent.
9. Pinch skin & insert needle: Gently pinch your skin at the chosen injection site.
Insert the entire needle into the pinched skin between your fingers, at a 45 to 90-degree angle.
DO NOT place your finger on the plunger while inserting the needle.
Hold the pre-filled syringe steady.
10. Inject: After inserting the needle, let go of the skin gently.
Press down the blue plunger until it can go no further. This activates the safety mechanism that will ensure full retraction of the needle after the injection is given.
A complete dose is administered if the blue plunger cannot go any further, and there are no spills.
11. Remove the used syringe: Remove the needle from the skin entirely before letting go of the blue plunger.
After the blue plunger is released, the safety lock will draw the needle inside the needle guard.
Dispose of used syringe in a sharps disposal container right away after use.
If there is some residual fluid or a tiny bit of blood, clean the injection site with a cotton ball or gauze pad WITHOUT applying any pressure. If you feel the need, you can use a sticky plaster to cover the injection site.

Immunosuppressants / Psoriasis, Seborrhea & Ichthyosis Preparations

L04AC17 - tildrakizumab ; Belongs to the class of interleukin inhibitors. Used as immunosuppressants.

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