Product Elements:
Klisyri tirbanibulin tirbanibulin tirbanibulin glyceryl mono and dipalmitostearate propylene glycol white to off-white
Indications and Usage:
1 indications and usage klisyri is indicated for the topical treatment of actinic keratosis on the face or scalp. klisyri is a microtubule inhibitor indicated for the topical treatment of actinic keratosis of the face or scalp. ( 1 )
Warnings and Cautions:
5 warnings and precautions may cause eye irritation upon ocular exposure. avoid transfer of the drug into the eyes and to the periocular area. if accidental exposure occurs, flush eyes with water and seek medical care. ( 5.1 ) local skin reactions can occur including severe reactions (e.g., vesiculation/pustulation, erosion/ulceration) in the treated area. avoid use until skin is healed from any previous drug or surgical treatment. ( 5.2 ) 5.1 ophthalmic adverse reactions klisyri may cause eye irritation. avoid transfer of the drug into the eyes and to the periocular area during and after application. wash hands immediately after application. if accidental exposure occurs, instruct patient to flush eyes with water and seek medical care as soon as possible. 5.2 local skin reactions local skin reactions, including severe reactions (erythema, flaking/scaling, crusting, swelling, vesiculation/pustulation and erosion/ulceration) in the treated area can occur after topical application of kli
Read more...syri [see adverse reactions ( 6.1 )] . avoid use until skin is healed from any previous drug, procedure, or surgical treatment. occlusion after topical application of klisyri is more likely to result in irritation.
Dosage and Administration:
2 dosage and administration for topical use only; not for oral or ophthalmic use. apply sufficient amount of klisyri to evenly cover up to 25 cm 2 treatment field on the face or scalp once daily for 5 consecutive days using 1 single-dose packet per application. wash hands immediately with soap and water after application. avoid washing and touching the treated area for approximately 8 hours after application of klisyri. following this time, the area may be washed with a mild soap. avoid transfer of klisyri to the periocular area [see warnings and precautions ( 5.1 )] . avoid application near and around the mouth and lips. for topical use; not for oral or ophthalmic use. ( 2 ) apply klisyri to the treatment field on the face or scalp once daily for 5 consecutive days using 1 single-dose packet per application. ( 2 )
Dosage Forms and Strength:
3 dosage forms and strengths ointment: 1% white to off-white ointment in a single-dose packet (2.5 mg tirbanibulin in 250 mg). ointment: 1% tirbanibulin, single-dose packets. ( 3 )
Contraindications:
4 contraindications none. none. ( 4 )
Adverse Reactions:
6 adverse reactions most common adverse reactions (incidence â¥2%) are local skin reactions, application site pruritus, and application site pain. ( 6.1 ) to report suspected adverse reactions, contact almirall, at 1-866-665-2782 or fda at 1-800-fda-1088 or www.fda.gov/medwatch . 6.1 clinical trials experience because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in clinical practice. two double-blind, vehicle-controlled clinical trials were conducted in 702 adult subjects with actinic keratosis on the face or scalp. subjects were randomized 1:1 to klisyri or vehicle. subjects enrolled in the trials had 4 to 8 clinically typical, visible, and discrete ak lesions in a contiguous area of 25 cm 2 on the face or scalp. subjects had an average age of 70 years (range 45 to 96 years) and were pr
Read more...edominantly caucasian (99%), male (87%), with fitzpatrick skin types i or ii (72%) and actinic keratosis on the face (68%) or scalp (32%). treatment groups were comparable across all demographics and baseline characteristics, including ak lesion count and distribution on the face or scalp. in the controlled trials, local skin reactions (lsrs) were collected independent of adverse events. local skin reactions including erythema, flaking/scaling, crusting, swelling, vesiculation/pustulation, erosions/ulcerations were assessed by the investigators using a grading scale of 0 = absent, 1 = mild (slightly, barely perceptible), 2 = moderate (distinct presence), and 3 = severe (marked, intense). the percentages of subjects with the maximal post-baseline grades for each local skin reaction greater than baseline by treatment group are provided in table 1 . lsrs were mostly mild to moderate in degree ( table 1 ). table 1 investigator assessment of maximal post-baseline local skin reactions greater than baseline in the treatment area (face or scalp) - pooled data from 2 controlled clinical phase 3 trials klisyri n = 353 vehicle n = 349 local skin reactions mild n (%) moderate n (%) severe n (%) mild n (%) moderate n (%) severe n (%) erythema 76 (22%) 223 (63%) 22 (6%) 98 (28%) 20 (6%) 0 flaking/ scaling 92 (26%) 166 (47%) 31 (9%) 86 (25%) 33 (9%) 1 (<1%) crusting 107 (30%) 50 (14%) 7 (2%) 31 (9%) 8 (2%) 0 swelling 102 (29%) 32 (9%) 2 (<1%) 15 (4%) 1 (<1%) 0 vesiculation/ pustulation 25 (7%) 2 (<1%) 2 (<1%) 3 (<1%) 0 0 erosion/ ulceration 32 (9%) 9 (3%) 0 10 (3%) 0 0 table 2 presents the adverse reactions experienced in â¥2% of subjects participating in the controlled clinical trials with klisyri. no subject withdrew from the trials due to adverse reactions. table 2 adverse reactions occurring in â¥2% of subjects in 2 controlled clinical trialsâ pooled safety population a application site pain includes pain, tenderness, stinging, and burning sensation at the application site. adverse reaction system organ class klisyri n = 353 vehicle n = 349 number of subjects (%) with any adverse reaction (possibly related to treatment) 56 (16%) 35 (10%) application site pruritus 32 (9%) 21 (6%) application site paina 35 (10%) 11 (3%) for the 51 subjects (45 klisyri, 6 vehicle) who maintained complete clearance through the 12-month follow-up period, no additional local adverse reactions were reported. dermal safety studies clinical studies in healthy subjects demonstrated klisyri did not cause contact sensitization (261 subjects), phototoxic skin reactions (31 subjects), or photoallergic skin reactions (64 subjects).
Adverse Reactions Table:
Table 1 Investigator Assessment of Maximal Post-Baseline Local Skin Reactions Greater Than Baseline in the Treatment Area (face or scalp) - Pooled Data from 2 Controlled Clinical Phase 3 Trials | KLISYRI N = 353 | Vehicle N = 349 |
| Local Skin Reactions | Mild n (%) | Moderate n (%) | Severe n (%) | Mild n (%) | Moderate n (%) | Severe n (%) |
| Erythema | 76 (22%) | 223 (63%) | 22 (6%) | 98 (28%) | 20 (6%) | 0 |
| Flaking/ Scaling | 92 (26%) | 166 (47%) | 31 (9%) | 86 (25%) | 33 (9%) | 1 (<1%) |
| Crusting | 107 (30%) | 50 (14%) | 7 (2%) | 31 (9%) | 8 (2%) | 0 |
| Swelling | 102 (29%) | 32 (9%) | 2 (<1%) | 15 (4%) | 1 (<1%) | 0 |
| Vesiculation/ Pustulation | 25 (7%) | 2 (<1%) | 2 (<1%) | 3 (<1%) | 0 | 0 |
| Erosion/ Ulceration | 32 (9%) | 9 (3%) | 0 | 10 (3%) | 0 | 0 |
Table 2 Adverse Reactions Occurring in ≥2% of Subjects in 2 Controlled Clinical Trials– Pooled Safety Population| a Application site pain includes pain, tenderness, stinging, and burning sensation at the application site. |
| Adverse Reaction System Organ Class | KLISYRI N = 353 | Vehicle N = 349 |
| Number of Subjects (%) with any adverse reaction (possibly related to treatment) | 56 (16%) | 35 (10%) |
| Application site pruritus | 32 (9%) | 21 (6%) |
| Application site paina | 35 (10%) | 11 (3%) |
Use in Specific Population:
8 use in specific populations 8.1 pregnancy risk summary there are no available data with klisyri use in pregnant women to evaluate for a drug-associated risk of major birth defects, miscarriage or adverse maternal or fetal outcomes. in animal reproduction studies, oral administration of tirbanibulin to pregnant rats during the period of organogenesis resulted in an increased incidence of fetal deaths and malformations at a systemic exposure that was at least 74 times the exposure associated with the maximum recommended human dose (mrhd). oral administration of tirbanibulin to pregnant rabbits during the period of organogenesis resulted in reduced mean fetal weight and size at a systemic exposure that was 159 times the exposure associated with the mrhd ( see data ). the background risk of major birth defects and miscarriage for the indicated population is unknown. all pregnancies have a background risk of birth defect, loss, or other adverse outcomes. in the u.s. general population, th
Read more...e estimated risk of major birth defects and miscarriage in clinically recognized pregnancies is 2 to 4% and 15 to 20%, respectively. data animal data tirbanibulin induced fetal deaths and external, visceral, and skeletal malformations when administered orally to pregnant rats during the period of organogenesis at doses greater than or equal to 1.25 mg/kg/day, which resulted in systemic exposures at least 74 times the exposure associated with the mrhd on an area under the curve (auc) comparison basis. tirbanibulin had no apparent effects on fetal development in rats at a dose of 0.5 mg/kg/day, which resulted in systemic exposures 18 times the exposure associated with the mrhd. tirbanibulin reduced mean fetal weight and size (crown-rump length) when administered orally to pregnant rabbits during the period of organogenesis at a dose of 3 mg/kg/day, which resulted in a systemic exposure 159 times the exposure associated with the mrhd on an auc comparison basis. tirbanibulin had no apparent effects on fetal development in rabbits at a dose of 1 mg/kg/day, which resulted in systemic exposures 53 times the exposure associated with the mrhd. tirbanibulin was assessed for effects on peri- and post-natal development of rats in a study that involved oral administration to pregnant rats during the period of organogenesis through lactation at dosages up to 1.25 mg/kg/day. these dosages resulted in systemic exposures up to 74 times the exposure associated with the mrhd on an auc comparison basis. no adverse effects on maternal function or developmental, neurobehavioral, or reproductive performance of offspring were observed. 8.2 lactation risk summary there are no data on lactational transfer of klisyri to human or animal milk. the effects of klisyri on the breastfed infant, or its effects on milk production, are unknown. the developmental and health benefits of breastfeeding should be considered along with the motherâs clinical need for klisyri and any potential adverse effects on the breastfed child from tirbanibulin or from the underlying maternal condition. 8.4 pediatric use the safety and effectiveness of klisyri for actinic keratosis in subjects less than 18 years of age have not been established. actinic keratosis is not a condition generally seen within the pediatric population. 8.5 geriatric use of the 353 subjects with ak treated with klisyri in the 2 controlled phase 3 trials, 246 (70%) were 65 years of age or older. no overall differences in safety or effectiveness were observed between these subjects and younger subjects, and other reported clinical experience has not identified differences in responses between the elderly and younger patients, but greater sensitivity of some older individuals cannot be ruled out.
Use in Pregnancy:
8.1 pregnancy risk summary there are no available data with klisyri use in pregnant women to evaluate for a drug-associated risk of major birth defects, miscarriage or adverse maternal or fetal outcomes. in animal reproduction studies, oral administration of tirbanibulin to pregnant rats during the period of organogenesis resulted in an increased incidence of fetal deaths and malformations at a systemic exposure that was at least 74 times the exposure associated with the maximum recommended human dose (mrhd). oral administration of tirbanibulin to pregnant rabbits during the period of organogenesis resulted in reduced mean fetal weight and size at a systemic exposure that was 159 times the exposure associated with the mrhd ( see data ). the background risk of major birth defects and miscarriage for the indicated population is unknown. all pregnancies have a background risk of birth defect, loss, or other adverse outcomes. in the u.s. general population, the estimated risk of major birt
Read more...h defects and miscarriage in clinically recognized pregnancies is 2 to 4% and 15 to 20%, respectively. data animal data tirbanibulin induced fetal deaths and external, visceral, and skeletal malformations when administered orally to pregnant rats during the period of organogenesis at doses greater than or equal to 1.25 mg/kg/day, which resulted in systemic exposures at least 74 times the exposure associated with the mrhd on an area under the curve (auc) comparison basis. tirbanibulin had no apparent effects on fetal development in rats at a dose of 0.5 mg/kg/day, which resulted in systemic exposures 18 times the exposure associated with the mrhd. tirbanibulin reduced mean fetal weight and size (crown-rump length) when administered orally to pregnant rabbits during the period of organogenesis at a dose of 3 mg/kg/day, which resulted in a systemic exposure 159 times the exposure associated with the mrhd on an auc comparison basis. tirbanibulin had no apparent effects on fetal development in rabbits at a dose of 1 mg/kg/day, which resulted in systemic exposures 53 times the exposure associated with the mrhd. tirbanibulin was assessed for effects on peri- and post-natal development of rats in a study that involved oral administration to pregnant rats during the period of organogenesis through lactation at dosages up to 1.25 mg/kg/day. these dosages resulted in systemic exposures up to 74 times the exposure associated with the mrhd on an auc comparison basis. no adverse effects on maternal function or developmental, neurobehavioral, or reproductive performance of offspring were observed.
Pediatric Use:
8.4 pediatric use the safety and effectiveness of klisyri for actinic keratosis in subjects less than 18 years of age have not been established. actinic keratosis is not a condition generally seen within the pediatric population.
Geriatric Use:
8.5 geriatric use of the 353 subjects with ak treated with klisyri in the 2 controlled phase 3 trials, 246 (70%) were 65 years of age or older. no overall differences in safety or effectiveness were observed between these subjects and younger subjects, and other reported clinical experience has not identified differences in responses between the elderly and younger patients, but greater sensitivity of some older individuals cannot be ruled out.
Overdosage:
10 overdosage overdose of klisyri could cause an increase in incidence and severity of local skin reactions.
Description:
11 description klisyri (tirbanibulin) ointment is a microtubule inhibitor for topical use. the chemical name of tirbanibulin is n -benzyl-2-(5-(4-(2-morpholinoethoxy)phenyl)pyridin-2-yl) acetamide. the molecular weight is 431.4 and the molecular formula is c 26 h 29 n 3 o 3 . tirbanibulinâs structural formula is: tirbanibulin ointment 1% contains 10 mg tirbanibulin per gram of white to off-white ointment containing mono- and di-glycerides and propylene glycol. chemical structure
Clinical Pharmacology:
12 clinical pharmacology 12.1 mechanism of action tirbanibulin is a microtubule inhibitor. the mechanism of action of klisyri for the topical treatment of actinic keratosis is unknown. 12.2 pharmacodynamics the pharmacodynamics of tirbanibulin in the treatment of actinic keratosis is unknown. 12.3 pharmacokinetics absorption following topical treatment of a mean daily dose of 138 mg (range: 54 to 295 mg) of klisyri to a 25 cm 2 contiguous area of the face or balding scalp, once daily for 5 consecutive days, the steady-state concentration of tirbanibulin was achieved by 72 hours with a mean±sd trough concentration (c trough ) of 0.11±0.08 ng/ml. on day 5, systemic exposure to tirbanibulin was low with a mean±sd maximum plasma concentration (c max ) of 0.34±0.30 ng/ml and 0.18±0.10 ng/ml, and a mean±sd area under the plasma concentration from time zero to 24 hours (auc 24 ) of 5.0±3.9 h*ng/ml and 3.2±1.9 h*ng/ml, in subjects who received the face and scalp topical
Read more... treatment, respectively. the median time to reach c max (t max ) was ~7 hours. distribution plasma protein binding of tirbanibulin is 88% and is independent of concentrations in the range of 0.01 to 10 µg/ml. elimination metabolism following topical treatment with klisyri to adult subjects with actinic keratosis, the plasma concentrations of kx2-5036 and kx2-5163, two pharmacologically inactive metabolites, were detectable with the highest plasma concentrations of 0.09 ng/ml and 0.12 ng/ml, respectively. the in vitro study indicated that incubation of 1 or 10 µm tirbanibulin with human hepatocytes generated kx2-5036, kx-5163 and other unidentified metabolites. in vitro, tirbanibulin is mainly metabolized by cyp3a4, and to a lesser extent, cyp2c8. excretion excretion of tirbanibulin has not been fully characterized in humans. drug interactions clinical studies no clinical studies evaluating the drug interaction potential of klisyri have been conducted. in vitro studies cyp enzymes: tirbanibulin and the metabolite kx2-5036 directly or time-dependently inhibited cyp 1a2, 2b6, 2c8, 2c9, 2c19, 2d6, or 3a4 with an ic 50 value of >17 µm. tirbanibulin up to 1 µm (431.5 ng/ml) and the metabolite kx2-5036 up to 3 µm (1024 ng/ml) did not induce cyp 1a2, 2b6, or 3a4. these findings suggest that klisyri has no clinically meaningful effect on the pk of drugs metabolized by cyp 1a2, 2b6, 2c8, 2c9, 2c19, 2d6, or 3a4. drug transporters: neither tirbanibulin nor the metabolite kx2-5036 was a substrate of mdr1, bcrp, bsep, mrp2, mate1, mate2-k, oat1, oat3, oatp1b1, oatp1b3, oct1 or oct2. tirbanibulin and the metabolite kx2-5036 inhibited mate1, mate2-k, oatp1b1, oatp1b3, oct1 and/or oct2 with an ic 50 value of >1 µm. the results suggest that klisyri has no clinically meaningful effect on the pk of drugs mediated by mate1, mate2-k, oatp1b1, oatp1b3, oct1 and oct2.
Mechanism of Action:
12.1 mechanism of action tirbanibulin is a microtubule inhibitor. the mechanism of action of klisyri for the topical treatment of actinic keratosis is unknown.
Pharmacodynamics:
12.2 pharmacodynamics the pharmacodynamics of tirbanibulin in the treatment of actinic keratosis is unknown.
Pharmacokinetics:
12.3 pharmacokinetics absorption following topical treatment of a mean daily dose of 138 mg (range: 54 to 295 mg) of klisyri to a 25 cm 2 contiguous area of the face or balding scalp, once daily for 5 consecutive days, the steady-state concentration of tirbanibulin was achieved by 72 hours with a mean±sd trough concentration (c trough ) of 0.11±0.08 ng/ml. on day 5, systemic exposure to tirbanibulin was low with a mean±sd maximum plasma concentration (c max ) of 0.34±0.30 ng/ml and 0.18±0.10 ng/ml, and a mean±sd area under the plasma concentration from time zero to 24 hours (auc 24 ) of 5.0±3.9 h*ng/ml and 3.2±1.9 h*ng/ml, in subjects who received the face and scalp topical treatment, respectively. the median time to reach c max (t max ) was ~7 hours. distribution plasma protein binding of tirbanibulin is 88% and is independent of concentrations in the range of 0.01 to 10 µg/ml. elimination metabolism following topical treatment with klisyri to adult subjects
Read more... with actinic keratosis, the plasma concentrations of kx2-5036 and kx2-5163, two pharmacologically inactive metabolites, were detectable with the highest plasma concentrations of 0.09 ng/ml and 0.12 ng/ml, respectively. the in vitro study indicated that incubation of 1 or 10 µm tirbanibulin with human hepatocytes generated kx2-5036, kx-5163 and other unidentified metabolites. in vitro, tirbanibulin is mainly metabolized by cyp3a4, and to a lesser extent, cyp2c8. excretion excretion of tirbanibulin has not been fully characterized in humans. drug interactions clinical studies no clinical studies evaluating the drug interaction potential of klisyri have been conducted. in vitro studies cyp enzymes: tirbanibulin and the metabolite kx2-5036 directly or time-dependently inhibited cyp 1a2, 2b6, 2c8, 2c9, 2c19, 2d6, or 3a4 with an ic 50 value of >17 µm. tirbanibulin up to 1 µm (431.5 ng/ml) and the metabolite kx2-5036 up to 3 µm (1024 ng/ml) did not induce cyp 1a2, 2b6, or 3a4. these findings suggest that klisyri has no clinically meaningful effect on the pk of drugs metabolized by cyp 1a2, 2b6, 2c8, 2c9, 2c19, 2d6, or 3a4. drug transporters: neither tirbanibulin nor the metabolite kx2-5036 was a substrate of mdr1, bcrp, bsep, mrp2, mate1, mate2-k, oat1, oat3, oatp1b1, oatp1b3, oct1 or oct2. tirbanibulin and the metabolite kx2-5036 inhibited mate1, mate2-k, oatp1b1, oatp1b3, oct1 and/or oct2 with an ic 50 value of >1 µm. the results suggest that klisyri has no clinically meaningful effect on the pk of drugs mediated by mate1, mate2-k, oatp1b1, oatp1b3, oct1 and oct2.
Nonclinical Toxicology:
13 nonclinical toxicology 13.1 carcinogenesis, mutagenesis, impairment of fertility no studies have been performed to evaluate the potential of tirbanibulin to induce carcinogenesis. tirbanibulin was negative in an in vitro bacterial reverse mutation (ames) assay. tirbanibulin was positive in an in vitro chromosomal aberration assay with chinese hamster ovary (cho) cells, an in vitro mouse lymphoma assay with l5178/tk +/- cells, and an in vivo micronucleus assay in rats. tirbanibulin was assessed for effects on fertility or reproductive function in rats. reproductive performance of rats was unaffected by oral doses of tirbanibulin up to 4 mg/kg/day (94 times the mrhd on an auc comparison basis) in males and 1 mg/kg/day (60 times the mrhd on an auc comparison basis) in females. however, oral administration of 4 mg/kg/day of tirbanibulin to male rats adversely affected spermatogenesis, including reduced sperm count and motility, and increased observations of morphologically abnormal sper
Read more...m. no effects on sperm were observed in males treated at 2 mg/kg/day (47 times the mrhd on an auc comparison basis).
Carcinogenesis and Mutagenesis and Impairment of Fertility:
13.1 carcinogenesis, mutagenesis, impairment of fertility no studies have been performed to evaluate the potential of tirbanibulin to induce carcinogenesis. tirbanibulin was negative in an in vitro bacterial reverse mutation (ames) assay. tirbanibulin was positive in an in vitro chromosomal aberration assay with chinese hamster ovary (cho) cells, an in vitro mouse lymphoma assay with l5178/tk +/- cells, and an in vivo micronucleus assay in rats. tirbanibulin was assessed for effects on fertility or reproductive function in rats. reproductive performance of rats was unaffected by oral doses of tirbanibulin up to 4 mg/kg/day (94 times the mrhd on an auc comparison basis) in males and 1 mg/kg/day (60 times the mrhd on an auc comparison basis) in females. however, oral administration of 4 mg/kg/day of tirbanibulin to male rats adversely affected spermatogenesis, including reduced sperm count and motility, and increased observations of morphologically abnormal sperm. no effects on sperm wer
Read more...e observed in males treated at 2 mg/kg/day (47 times the mrhd on an auc comparison basis).
Clinical Studies:
14 clinical studies actinic keratosis of the face or scalp two double-blind, vehicle-controlled clinical trials (nct03285477 and nct03285490) were conducted with 702 adult subjects with actinic keratosis on the face or scalp. subjects were randomized 1:1 to klisyri or vehicle. subjects enrolled had 4 to 8 clinically typical, visible, and discrete ak lesions in a contiguous area of 25 cm 2 on the face or scalp. subjects had an average age of 70 years (range 45 to 96 years), were predominantly caucasian (99%), male (87%), with fitzpatrick skin types i or ii (72%) and actinic keratosis on the face (68%) or scalp (32%). treatment groups were comparable across all demographics and baseline characteristics, including ak lesion count and distribution on the face or scalp. subjects received 5 consecutive days of once daily treatment with either klisyri (353) or vehicle control (349) to the treatment field. subjects with complete (100%) clearance of ak lesions in the treatment area at day 57 re
Read more...turned to the clinic for recurrence assessment every 3 months for a total of 12 months post-day 57. the primary efficacy endpoint was complete (100%) clearance of ak lesions in the treatment area, defined as the proportion of subjects at day 57 with no clinically visible ak lesions in the treatment area and the secondary endpoint was partial (â¥75%) clearance of ak lesions in the treatment area. results from both studies are presented below. table 3 complete (100%) ak clearance rates on day 57 for the two phase 3 studies (intent to treat [itt] population a. based on mantel-haenszel method study 1 study 2 klisyri n = 175 n/n (%) vehicle n = 176 n/n (%) treatment difference (klisyri-vehicle) 95% confidence interval for the treatment difference klisyri n = 178 n/n (%) vehicle n = 173 n/n (%) treatment difference (klisyri-vehicle) 95% confidence interval for the treatment difference all subjects 77/175 (44%) 8/176 (5%) 40% a (31.6%, 47.5%) a 97/178 (54%) 22/173 (13%) 42% a (33.1%, 50.7%) a face 60/119 (50%) 7/121 (6%) 45% -- 73/119 (61%) 16/118 (14%) 48% -- scalp 17/56 (30%) 1/55 (2%) 29% -- 24/59 (41%) 6/55 (11%) 30% -- table 4 partial (⥠75%) ak clearance rates on day 57 for the two phase 3 studies (intent to treat [itt] population) a. based on mantel-haenszel method study 1 study 2 klisyri n = 175 n/n (%) vehicle n = 176 n/n (%) treatment difference (klisyri-vehicle) 95% confidence interval for the treatment difference klisyri n = 178 n/n (%) vehicle n = 173 n/n (%) treatment difference (klisyri-vehicle) 95% confidence interval for the treatment difference all subjects 119/175 (68%) 29/176 (16%) 52% a (42.9%, 60.3%) a 136/178 (76%) 34/173 (20%) 57% a (48.3%, 65.4%) a face 90/119 (76%) 23/121 (19%) 57% -- 95/119 (80%) 26/118 (22%) 58% -- scalp 29/56 (52%) 6/55 (11%) 41% -- 41/59 (69%) 8/55 (15%) 55% -- efficacy was consistent across sex and age (<65 and â¥65 years) subgroups. subjects who achieved 100% clearance of ak lesions in the treatment area at day 57 continued to be followed for up to 12 months following day 57 to determine the recurrence rate. recurrence was defined as the proportion of subjects with any identified ak lesion (new or previous lesion) in the previously treated area who achieved 100% clearance at day 57. of the 174 subjects treated with klisyri who were followed, the recurrence rate at 12 months post day 57 was 73%.
How Supplied:
16 how supplied/storage and handling klisyri is a white to off-white ointment and is supplied in packets containing 250 mg of tirbanibulin ointment 1%. each packet should be discarded after single use. ndc 16110-391-05 (5 single-dose packets) store at 20°c-25°c (68°f-77°f), excursions permitted to 15°c-30°c (59°f-86°f) [see usp controlled room temperature]. do not refrigerate or freeze.
Information for Patients:
17 patient counseling information advise the patient to read the fda-approved patient labeling ( patient information and instructions for use). discard the packet after a single use. ophthalmic adverse reactions advise patients that klisyri is not for ophthalmic use. advise patients to avoid application around the eyes, and transfer of the drug into the eyes and to the periocular area. if accidental exposure occurs, advise patients to flush eyes with water and seek medical care [see warnings and precautions ( 5.1 )] . local skin reactions inform patients that treatment with klisyri may lead to local skin reactions [see warnings and precautions ( 5.3 )] . important administration instructions advise patients that klisyri is for topical use only. advise patients to avoid application near and around the eyes, mouth and lips. instruct patients to: wash hands well after applying klisyri to avoid transfer of the drug into the eyes and to the periocular area after application. avoid washing a
Read more...nd touching the treated area for 8 hours after treatment. following this time, patients may wash the area with a mild soap and water. avoid inadvertent transfer of klisyri to other areas, or to another person. manufactured for: almirall, llc malvern, pa. 19355, usa revised: 08/2021
Spl Patient Package Insert:
This patient information has been approved by the u.s. food and drug administration. issued: 08/2021 patient information klisyri (klye si' ree) (tirbanibulin) ointment important: klisyri is for use on the skin only (topical). do not use klisyri in, around, or near your eyes, mouth or lips. what is klisyri? klisyri is a prescription medicine used on the skin to treat actinic keratosis on the face or scalp. it is not known if klisyri is safe and effective in children less than 18 years of age. before using klisyri, tell your healthcare provider about all of your medical conditions, including if you: are being treated or have been treated for actinic keratosis with any other medicine, procedure, or surgery. you should not use klisyri until your skin has healed from other treatments. have other skin problems in the treatment area. are pregnant or plan to become pregnant. it is not known if klisyri can harm your unborn baby. are breastfeeding or plan to breastfeed. it is not known if klisyr
Read more...i passes into your breast milk. talk to your healthcare provider about the best way to feed your baby during treatment with klisyri. tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins and herbal supplements. how should i use klisyri? use klisyri as your healthcare provider tells you to. klisyri is for skin use only. apply klisyri to evenly cover the treatment area(s) on the face or scalp 1 time a day for 5 days in a row (consecutive) using 1 single dose packet with each application. do not apply klisyri to other areas. do not use more klisyri than you need to cover the treatment area. using too much klisyri, or using it too often, or for too long can increase your chances of having a severe skin reaction or other side effects. do not cover the treatment area with a dressing after application of klisyri. irritation of the skin may happen if a dressing is applied to the treatment area. do not get klisyri in, around, or near your eyes. do not touch your eyes while you are applying klisyri. wash your hands right away with water and soap after applying klisyri. after applying klisyri, be careful to keep klisyri on the treated area from coming into contact with your eyes. irritation may happen if you get klisyri in your eyes. if you accidently get klisyri in your eyes, flush them with water and get medical care as soon as possible. see, â what are the possible side effects of klisyri? â do not get klisyri in, around, or near your mouth or lips. avoid washing and touching the treated area for approximately 8 hours after application of klisyri. after 8 hours, you may wash the area with a mild soap and water. avoid transferring the product to other areas after application. throw away any open packet of klisyri after use even if there is medicine still left in it. what are the possible side effects of klisyri? klisyri may cause serious side effects, including: eye irritation can happen if klisyri gets into your eyes. if you accidently get klisyri into your eyes, flush them with water and get medical care as soon as possible. local skin reactions are common but can also be severe during treatment with klisyri. call your healthcare provider if you develop any local skin reactions including redness, flaking or scaling, crusting, or swelling that is more severe, or if you get blisters, peeling, pus, ulcers, or breakdown of your skin. the most common side effects of klisyri include: itching or pain in the treatment area. these are not all of the possible side effects of klisyri. call your doctor for medical advice about side effects. you may report side effects to fda at 1-800-fda-1088. how should i store klisyri? store at room temperature between 68°f to 77°f (20°c to 25°c) . do not refrigerate or freeze. safely throw away used klisyri packets in household trash. keep klisyri and all medicines out of the reach of children. general information about the safe and effective use of klisyri. medicines are sometimes prescribed for purposes other than those listed in a patient information leaflet. do not use klisyri for a condition for which it was not prescribed. do not give klisyri to other people, even if they have the same symptoms you have. it may harm them. you can ask your pharmacist or healthcare provider for information about klisyri that is written for health professionals. what are the ingredients of klisyri? active ingredient: tirbanibulin inactive ingredients: mono- and di-glycerides and propylene glycol. manufactured for: almirall, llc, malvern, pa. 19355, usa. for more information, call 1-800-klisyri or visit www.klisyri.com .
Package Label Principal Display Panel:
Principal display panel - ndc: 16110-391-05 - packet label packet label
Principal display panel - ndc: 16110-391-05 - carton label carton label