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Ritlecitinib

Phase 3

Alopecia Areata | Small molecule | Dermatology |Pfizer, Inc.|Last Updated: Sep 1, 2026

Target and mechanism

Molecular targetJAK3, ITK, BMX, TEC, TXK, BTK
Target classInhibitor
ModalitySmall molecule

Also known as Ritlecitinib higher dose

Success Probability

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Market & Valuation

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Trial Design

RandomizedDouble-BlindNO_TREATMENT_CONTROLLEDDMC
Total Trials3
Total Enrollment1,681

FDA Designations

No designations recorded

Clinical trial landscape

Ritlecitinib · 14 trials · 11 indications

Phase 3 5Phase 2 2Phase 1 7
NCT07733765A Study in Young People and Adults to Learn About the Medicine Ritlecitinib for Treatment of Patchy Hair Loss, Known by the Medical Term as Moderate Alopecia AreataAlopecia Areata
RECRUITING336 Analytics
NCT06873945A Study of 2 Doses of Ritlecitinib in People 12 Years of Age and Older With Alopecia AreataAlopecia Areata
RECRUITING1,330 Analytics
NCT06163326A 52-Week Study to Learn About the Safety and Effects of Ritlecitinib in Participants With Nonsegmental VitiligoVitiligo
ACTIVE NOT_RECRUITING394 Analytics
NCT06072183A 104-Week Study of Ritlecitinib Oral Capsules in Adults With Nonsegmental Vitiligo (Active and Stable) Tranquillo 2Stable Nonsegmental Vitiligo
ACTIVE NOT_RECRUITING1,571 Analytics
NCT05583526A 52-Week Study of Ritlecitinib Oral Capsules in Adults and Adolescents With Nonsegmental Vitiligo (Active and Stable) TranquilloStable Nonsegmental Vitiligo
COMPLETED607 Analytics
PHASE3RECRUITING
A Study in Young People and Adults to Learn About the Medicine Ritlecitinib for Treatment of Patchy Hair Loss, Known by the Medical Term as Moderate Alopecia Areata
Alopecia AreataUnlock trial analytics
PHASE3RECRUITING
A Study of 2 Doses of Ritlecitinib in People 12 Years of Age and Older With Alopecia Areata
Alopecia AreataUnlock trial analytics
PHASE3ACTIVE NOT_RECRUITING
A 52-Week Study to Learn About the Safety and Effects of Ritlecitinib in Participants With Nonsegmental Vitiligo
VitiligoUnlock trial analytics
PHASE3ACTIVE NOT_RECRUITING
A 104-Week Study of Ritlecitinib Oral Capsules in Adults With Nonsegmental Vitiligo (Active and Stable) Tranquillo 2
Stable Nonsegmental VitiligoUnlock trial analytics
PHASE3COMPLETED
A 52-Week Study of Ritlecitinib Oral Capsules in Adults and Adolescents With Nonsegmental Vitiligo (Active and Stable) Tranquillo
Stable Nonsegmental VitiligoUnlock trial analytics

Study Endpoints

Primary Endpoints

Difference in the proportion of Severity of Alopecia Tool (SALT) 0 responders at Week 24 between ritlecitinib 50 mg QD versus placebo
Week 24
Part 1: Percentage of participants with absolute Severity of Alopecia Tool (SALT) score less than or equal to 20
Week 24

Difference in the percentage of participants with SALT score less than or equal to 20 between ritlecitinib 100 mg once-daily (QD) versus placebo

Part 2: Percentage of participants with TEAEs, SAEs, and AEs leading to discontinuation
Baseline to Follow-up visit (Week 52)

Percentage of participants with events, based on those reported in the study including the safety follow-up period for ritlecitinib 100 mg QD

Part 2: Percentage of participants with clinically significant laboratory abnormalities
Baseline to Follow-up visit (Week 52)

Percentage of participants with clinically significant laboratory abnormalities, based on those reported in the study including the safety follow-up period for ritlecitinib 100 mg QD

Incidence of treatment-emergent adverse events (TEAEs), serious adverse events (SAEs), and adverse events (AEs) leading to discontinuation
Screening up to at least 30 days after last dose of study drug (week 52 or Early Termination)

To evaluate the long-term safety and tolerability of ritlecitinib in adult and adolescent participants with non-segmental vitiligo

Incidence of clinically significant laboratory abnormalities
Screening up to at least 30 days after last dose of study drug (week 52 or Early Termination)

To evaluate the long-term safety and tolerability of ritlecitinib in adult and adolescent participants with non-segmental vitiligo

US only Co-Primary Endpoints: Response based on Facial Vitiligo Area Scoring Index 75 (F-VASI75) at Week 52 and Total body Vitiligo Area Scoring Index 50 (T-VASI50) at Week 52
52 Weeks

Proportion of participants achieving F-VASI75 (defined as at least 75% improvement in F-VASI from Baseline) and T-VASI50 (defined as at least 50% improvement in T-VASI from Baseline)

Global (Other than US): Response based on Facial Vitiligo Area Scoring Index 75 (F-VASI75) at Week 52
52 Weeks

Proportion of participants achieving F-VASI75 (defined as at least 75% improvement in F-VASI from Baseline).

Incidence of Treatment Emergent Adverse Events (TEAEs), Serious Adverse Events (SAEs) and Adverse Events (AEs) leading to discontinuation.
Baseline through 108 weeks

To evaluate the safety and tolerability of ritlecitinib in adult participants with non segmental vitiligo

Incidence of Clinically significant laboratory abnormalities.
Baseline through 108 weeks
US only Co-Primary Endpoints: Response based on Facial Vitiligo Area Scoring Index 75 (F-VASI75) at Week 52 and T-VASI50 at Week 52
Week 52

Proportion of participants achieving F-VASI75 (defined as at least 75% improvement in F-VASI from Baseline) and T-VASI50 (defined as at least 50% improvement in T-VASI from Baseline)

Incidence of Treatment Emergent Adverse Events (TEAEs), Serious Adverse Events (SAEs), Adverse Events (AEs), leading to discontinuation, and clinically significant laboratory abnormalities
Baseline through Week 52

Safety and tolerability of ritlecitinib in participants with nonsegmental vitiligo

Difference in proportion of responders based on Hidradenitis Suppurativa Clinical Response achieving at least 50% reduction from baseline (Hidradenitis Suppurativa Clinical Response HiSCR50) in patients with HS treated with ritlecitinib versus placebo.
Week 16

The difference in proportion of responders based on HiSCR50 response at Week 16 in patients with HS treated with ritlecitinib versus placebo.

Change from baseline in Urticaria Activity Score 7 (UAS7) at Week 12
Week 12
Incidence of Treatment Emergent Adverse Events, Serious Adverse Events, and Adverse Events leading to discontinuation
Week 12
Site of capsule disintegration and MR microsphere dispersion
up to 48 hours post dose or as long as radioactivity is present in the GI tract (if it is shorter than 48 hours)

The time and gastrointestinal location where the HPMC capsule(s) disintegrate and disperse the drug formulation.

Gastric emptying time
up to 48 hours post dose or as long as radioactivity is present in the GI tract (if it is shorter than 48 hours)

Gastric emptying metrics may include a) time of 1st GE; b) time(s) for GE 10%, 25%, 50%, 75%, 90% and complete gastric emptying time GE100%.

Small intestine residence/transit time
up to 48 hours post dose or as long as radioactivity is present in the GI tract (if it is shorter than 48 hours)

Small Intestine transit metrics may include time for 10%, 25%, 50%, 75%, 90% and 100% of the formulation to transit through the small intestine.

Colon arrival time
up to 48 hours post dose or as long as radioactivity is present in the GI tract (if it is shorter than 48 hours)

Arrival time at the colon (ATC) metrics may include a) time(s) for ATC 10%, 25%, 50%, 75%, 90% and 100%.

Colon (ascending, transverse, descending) residence/transit time
up to 48 hours post dose or as long as radioactivity is present in the GI tract (if it is shorter than 48 hours)

The residence time of the formulation in the three primary regions of the large intestine to include the ascending, transverse and descending colon.

Total transit time
up to 48 hours post dose or as long as radioactivity is present in the GI tract (if it is shorter than 48 hours)

Residence time of the formulation in the gastrointestinal tract.

Maximum Observed Concentration (Cmax) of Ritlecitinib: MR Capsules vs Oral Solution Under Fasted Condition
For oral solution: Pre-dose (0 hours), 0.5, 1, 2, 3, 4, 6, 10, 12 and 24 hours post-dose on Day 1 of Period 1, 2 or 3; for MR1 and MR2 capsules: Pre-dose (0 hours), 1, 2, 3, 4, 6, 10, 12,16, 24, 36 and 48 hours post-dose on Day 1 of Period 1, 2 or 3
Area Under the Plasma Concentration-Time Profile From Time Zero (0) Extrapolated to Infinite Time (AUCinf) of Ritlecitinib: MR Capsules vs Oral Solution Under Fasted Condition
For oral solution: Pre-dose (0 hours), 0.5, 1, 2, 3, 4, 6, 10, 12 and 24 hours post-dose on Day 1 of Period 1, 2 or 3; for MR1 and MR2 capsules: Pre-dose (0 hours), 1, 2, 3, 4, 6, 10, 12,16, 24, 36 and 48 hours post-dose on Day 1 of Period 1, 2 or 3

AUCinf was calculated as AUClast + (Clast/kel), where Clast was the predicted plasma concentration at the last quantifiable time point from the log-linear regression analysis and kel was the terminal phase rate constant calculated by a linear regression of the log-linear concentration-time curve.

Area Under the Plasma Concentration-Time Profile From Time Zero Extrapolated to Infinite Time (AUCinf) of Ritlecitinib
0 (pre-dose), 0.25, 0.5, 1, 1.5, 2, 3, 4, 6, 9, 12 and 24 hours post-dose on Day 1 of each period. Each treatment period lasted 24 hours. Dosing of each period was separated by at least a 48-hour washout interval.

AUCinf was defined as area under the plasma-concentration time profile from time zero extrapolated to infinite time. AUCinf for ritlecitinib was calculated by AUClast + (Clast/kel), where Clast was the predicted plasma concentration at the last quantifiable time point from the log-linear regression analysis and kel was the terminal phase rate constant calculated by a linear regression of the log-linear concentration time curve.

Maximum Observed Concentration (Cmax) of Ritlecitinib
0 (pre-dose), 0.25, 0.5, 1, 1.5, 2, 3, 4, 6, 9, 12 and 24 hours post-dose on Day 1 of each period. Each treatment period lasted 24 hours. Dosing of each period was separated by at least a 48-hour washout interval.

Cmax was defined as maximum observed plasma concentration. Cmax for ritlecitinib was observed directly from data.

Area Under the Plasma Concentration-Time Profile Over the Dosing Interval of 24 Hours, at Steady State (AUC24ss/AUCtau) of Ritlecitinib on Day 7
Day 7: 0 (pre-dose), 0.5, 1, 3, 8 and 24 hours [pre-dose concentration was used as an estimate for the concentration of 24 hours post dose]

Linear-log trapezoidal method was used for evaluation. For the calculation of AUCtau, pre-dose concentration of Day 7 was used as an estimate for the concentration of 24 hours post-dose on Day 7.

Maximum Plasma Concentration (Cmax) of Tolbutamide Administered With and Without Ritlecitinib
Pre-dose, 0.5, 1, 2, 3, 4, 5, 6, 8, 12, 16, 24, and 36 hours post-dose of tolbutamide in Period 1 (Days 1 and 2) and Period 2 (Days 10 and 11)

Cmax was defined as maximum observed plasma concentration. The determination method of Cmax was observing directly from data.

Area Under the Plasma Concentration Time Profile From Time Zero Extrapolated to Infinite Time (AUCinf) of Tolbutamide Administered With and Without Ritlecitinib
Pre-dose, 0.5, 1, 2, 3, 4, 5, 6, 8, 12, 16, 24, and 36 hours post-dose in Period 1 (Days 1 and 2) and Period 2 (Days 10 and 11)

AUCinf was defined as area under the plasma concentration time profile from time 0 extrapolated to infinite time.

Percent Target Occupancy for JAK3
-1 (pre-dose), 0 (pre-dose), 1, 2, 4, 8, 24, 48 hours post-dose

Target occupancy for janus kinase 3 (JAK3) in peripheral blood mononuclear cells (PBMCs) by ritlecitinib was investigated in human blood by chemical probe-based enrichment and liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS) analysis. % TO is calculated as \[(baseline value - value at specified time point)\*100/baseline value\], where baseline value in this formula is defined as the mean of the two pre-dose measurements at Hour -1 and Hour 0 on Day 1. Since (baseline value - value at specified time point)=0 at baseline, % TO at baseline is 0.

Percent Target Occupancy for BTK
-1 (pre-dose), 0 (pre-dose), 1, 2, 4, 8, 24, 48 hours post-dose

Target occupancy for Bruton's tyrosine kinase (BTK) in PBMCs by ritlecitinib was investigated in human blood by chemical probe-based enrichment and LC-MS/MS analysis. % TO is calculated as \[(baseline value - value at specified time point)\*100/baseline value\], where baseline value in this formula is defined as the mean of the two pre-dose measurements at Hour -1 and Hour 0 on Day 1. Since (baseline value - value at specified time point)=0 at baseline, % TO at baseline is 0.

Percent Target Occupancy for ITK
-1 (pre-dose), 0 (pre-dose), 1, 2, 4, 8, 24, 48 hours post-dose

Target occupancy forIL 2 inducible T-cell kinase (ITK) in PBMCs by ritlecitinib was investigated in human blood by chemical probe-based enrichment and LC-MS/MS analysis. % TO is calculated as \[(baseline value - value at specified time point)\*100/baseline value\], where baseline value in this formula is defined as the mean of the two pre-dose measurements at Hour -1 and Hour 0 on Day 1. Since (baseline value - value at specified time point)=0 at baseline, % TO at baseline is 0.

Percent Target Occupancy for TXK
-1 (pre-dose), 0 (pre-dose), 1, 2, 4, 8, 24, 48 hours post-dose

Target occupancy for tyrosine kinase expressed in T cells (TXK) in PBMCs by ritlecitinib was investigated in human blood by chemical probe-based enrichment and LC-MS/MS analysis. % TO is calculated as \[(baseline value - value at specified time point)\*100/baseline value\], where baseline value in this formula is defined as the mean of the two pre-dose measurements at Hour -1 and Hour 0 on Day 1. Since (baseline value - value at specified time point)=0 at baseline, % TO at baseline is 0.

Percent Target Occupancy for TEC
-1 (pre-dose), 0 (pre-dose), 1, 2, 4, 8, 24, 48 hours post-dose

Target occupancy for tyrosine kinase expressed carcinoma (TEC) in PBMCs by ritlecitinib was investigated in human blood by chemical probe-based enrichment and LC-MS/MS analysis. % TO is calculated as \[(baseline value - value at specified time point)\*100/baseline value\], where baseline value in this formula is defined as the mean of the two pre-dose measurements at Hour -1 and Hour 0 on Day 1. Since (baseline value - value at specified time point)=0 at baseline, % TO at baseline is 0.

Percent Target Occupancy for BMX
-1 (pre-dose), 0 (pre-dose), 1, 2, 4, 8, 24, 48 hours post-dose

Target occupancy for bone marrow tyrosine kinase gene in chromosome X (BMX) in PBMCs by ritlecitinib was investigated in human blood by chemical probe-based enrichment and LC-MS/MS analysis. % TO is calculated as \[(baseline value - value at specified time point) \*100/baseline value\], where baseline value in this formula is defined as the mean of the two pre-dose measurements at Hour -1 and Hour 0 on Day 1. Since (baseline value - value at specified time point)=0 at baseline, % TO at baseline is 0.

Area Under the Plasma Concentration-Time Profile From Time 0 Extrapolated to Infinite Time (AUCinf) for Ritlecitinib
Pre-dose, 0.25, 0.5, 1, 1.5, 2, 3, 4, 6, 9, 12, 16, and 24 hours post dose on Day 1 in each period

Plasma AUCinf for ritlecitinib is reported. AUCinf was calculated as \[AUClast+(Clast\*/kel)\], where AUClast is the area under the plasma concentration-time profile from time 0 to the time of the Clast, Clast is the last quantifiable concentration, Clast\* is the predicted plasma concentration at the last quantifiable time point estimated from the log-linear regression analysis, and kel is the terminal phase rate constant calculated by a linear regression of the log-linear concentration-time curve.

Maximum Plasma Concentration (Cmax) for Ritlecitinib
Pre-dose, 0.25, 0.5, 1, 1.5, 2, 3, 4, 6, 9, 12, 16, and 24 hours post dose on Day 1 in each period

Plasma Cmax for ritlecitinib is reported.

Secondary Endpoints

Difference in the proportion of SALT ≤5 responders at Week 24 between ritlecitinib 50 mg QD versus
Week 24
Difference in the proportion of SALT ≤10 responders at Week 24 between ritlecitinib 50 mg QD versus
Week 24
Difference in the proportion of SALT 75 responders at Week 24 between ritlecitinib 50 mg QD versus
Week 24
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Study Design & Arms

AllocationRANDOMIZED
MaskingQUADRUPLE
ModelPARALLEL
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
Ritlecitinib 50 milligrams (mg)EXPERIMENTALParticipants will receive 1 ritlecitinib 50 mg capsule QD orally from Day 1 to Week 24. At Week 24: Responders will be allocated to the below: Arm 1A (Ritlecitinib 50 mg R Group): 1 ritlecitinib 50 mg capsule QD and 1 placebo 100 mg capsule QD orally through Week 48. Non-Responders will be re-randomized to either of the below: Arm 1B (Ritlecitinib 50 mg NR→50 mg Group): 1 ritlecitinib 50 mg capsule QD and 1 placebo 100 mg capsule QD orally through Week 48. Arm 1C (Ritlecitinib 50 mg NR→100 mg Group): 1 ritlecitinib 100 mg capsule QD and 1 placebo 50 mg capsule QD orally through Week 48.
PlaceboPLACEBO_COMPARATORParticipants will receive 1 placebo 50 mg capsule QD orally from Day 1 to Week 24 At Week 24: Responders will be allocated to the below: Arm 2A (Placebo R Group): 1 placebo 50 mg capsule QD and 1 placebo 100 mg capsule QD orally through Week 48. Non-Responders will be allocated to the below: Arm 2B (Placebo NR→Ritlecitinib 50 mg Group): 1 ritlecitinib 50 mg capsule QD and 1 placebo 100 mg capsule QD orally through Week 48.
Ritlecitinib 50 mgEXPERIMENTALParticipants in Part 1 will be randomized to Ritlecitinib 50 mg QD for 24 weeks. Depending on response status at Week 24 (ie, whether the participant has a SALT score of less than or equal to 20), the participant may be re-randomized to Ritlecitinib 50 mg QD or Ritlecitinib 100 mg QD for another 24 weeks. Data from participants who are non-responders (ie, had a SALT score greater than 20) at Week 24 and re-randomized to Ritlecitinib 50 mg will be augmented with data from an External Ritlecitinib 50 mg QD Group for comparisons at Week 48. The External Ritlecitinib 50 mg QD Group will be constructed using patient-level data from the appropriately chosen Pfizer clinical study in participants who received Ritlecitinib 50 mg QD and were non-responders at Week 24 and continued receiving ritlecitinib 50 mg QD up to Week 48. In addition to the active Ritlecitinib 50 mg capsule, a placebo capsule matching the Ritlecitinib 100 mg capsule will be given in order to maintain the blind.
External PlaceboNO_INTERVENTIONThis group will be constructed using participant-level data at Week 24 from placebo groups of the appropriately chosen Pfizer clinical studies of Ritlecitinib in participants with alopecia areata. This data will be used for comparison between each Ritlecitinib dose and placebo at Week 24. As this arm will utilize data from other studies, no participants will be randomized to receive only placebo in this study.
Ritlecitinib 100 mgEXPERIMENTALParticipants in Part 1 will be randomized to Ritlecitinib 100 mg QD for 48 weeks. In addition to the active Ritlecitinib 100 mg capsule, a placebo capsule matching the Ritlecitinib 50 mg capsule will be given in order to maintain the blind.
Synthetic PlaceboNO_INTERVENTIONThis group will be constructed using participant-level data up to Week 36 from the placebo groups of the appropriately chosen Pfizer clinical studies of Ritlecitinib in participants with alopecia areata and a longitudinal model and extrapolation. This data will be used for comparison between Ritlecitinib 100 mg and placebo at Week 36. As this arm will utilize data from other studies, no participants will be randomized to receive only placebo in this study.
Ritlecitinib 100 mg (open-label)EXPERIMENTALParticipants in Part 2 will be assigned to receive one open-label Ritlecitinib 100 mg capsule once daily by mouth for 48 weeks.
Arm 1EXPERIMENTALParticipants who previously received 1 ritlecitinib 50 mg capsule QD orally from BL to Week 52 in Study B7981040. Ritlecitinib 50 mg or Ritlecitinib 100 mg or Placebo will be assigned.
Arm 2EXPERIMENTALParticipants who previously received 1 placebo 50 mg capsule QD orally from BL to Week 52 in Study B7981040 Ritlecitinib 50 mg or Ritlecitinib 100 mg or Placebo will be assigned
Arm 1- Ritlecitinib 100 milligrams (mg)EXPERIMENTALRandomized to Ritlecitinib 100 mg QD for 52 weeks before progressing into the up/down titration extension period, rerandomized according to responder status.
Arm 2- Ritlecitinib 50mgEXPERIMENTALRandomized to Ritlecitinib 50 mg QD for 52 weeks before progressing into the up/down titration extension period, rerandomized according to responder status.
Arm 3- PlaceboPLACEBO_COMPARATORRandomized to Placebo QD for 52 weeks before progressing into the up/down titration extension period, rerandomized according to responder status.
Arm 4- Ritlecitinib 100mgEXPERIMENTALNon-randomized open-label Ritlecitinib 100mg QD for 52 weeks.
Study InterventionEXPERIMENTALParticipants will receive one oral dose once daily (QD), starting with a loading dose of ritlecitinib for 8 weeks, followed by maintenance for 8 weeks.
Arm 3PLACEBO_COMPARATORRandomized to placebos matching the Ritlecitinib 50 mg and Ritlecitinib 100 mg capsules will be given to maintain blind from Day 1 to Week 12 (Period A). From Week 12 to Week 24 (Period B), will be switched to Ritlecitinib 100 mg. In addition to the active Ritlecitinib 100 mg capsule, a placebo matching the Ritlecitinib 50 mg capsule will be given to maintain blind.
Treatment Sequence 1EXPERIMENTALRitlecitinib 100 mg solution (fasted, Period 1), followed by ritlecitinib 100 mg MR capsule with 153Sm2O3 (fasted, Period 2), and followed by ritlecitinib 100 mg MR capsule with 153Sm2O3 (fed, Period 3).
Treatment Sequence 2EXPERIMENTALRitlecitinib 100 mg solution (fasted, Period 1), followed by ritlecitinib 100 mg MR capsule with 153Sm2O3 (fed, Period 2), and followed by ritlecitinib 100 mg MR capsule with 153Sm2O3 (fasted, Period 3).
Treatment Sequence 3EXPERIMENTALRitlecitinib 100 mg MR capsule 2 (fasted, Period 1), followed by ritlecitinib 100 mg solution (fasted, Period 2), followed by ritlecitinib 100 mg MR capsule 1 (fasted, Period 3), and followed by ritlecitinib 100 mg MR capsule 1 (fed, Period 4)
Treatment Sequence 4EXPERIMENTALRitlecitinib 100 mg solution (fasted, Period 1), followed by ritlecitinib 100 mg MR capsule 1 (fasted, Period 2), followed by ritlecitinib 100 mg MR capsule 2 (fasted, Period 3), and followed by ritlecitinib 100 mg MR capsule 2 (fed, Period 4)
Treatment Sequence 5EXPERIMENTALRitlecitinib 100 mg MR capsule 1 (fasted, Period 1), followed by ritlecitinib 100 mg MR capsule 2 (fasted, Period 2), followed by ritlecitinib 100 mg solution (fasted, Period 3), and followed by ritlecitinib 100 mg MR capsule 2 (fed, Period 4)
Treatment Sequence 6EXPERIMENTALRitlecitinib 100 mg MR capsule 2 (fasted, Period 1), followed by ritlecitinib 100 mg solution (fasted, Period 2), followed by ritlecitinib 100 mg MR capsule 1 (fasted, Period 3), and followed by ritlecitinib 100 mg MR capsule 2 (fed, Period 4)
Treatment AACTIVE_COMPARATORritlecitinib 1 x 30 milligram (mg) intact blend-in-capsule (BiC) in fasted state
Treatment BACTIVE_COMPARATORcontents of ritlecitinib 1 x 30 mg intact BiC sprinkled on strawberry jam in fasted state
Treatment CACTIVE_COMPARATORcontents of ritlecitinib 1 x 30 mg intact BiC sprinkled on yoghurt in fasted state
Treatment DACTIVE_COMPARATORcontents of ritlecitinib 1 x 30 mg intact BiC sprinkled on applesauce in fasted state
Treatment EACTIVE_COMPARATORritlecitinib 1 x 30 mg intact BiC given with high fat meal
Ritlecitinib 20 mgEXPERIMENTALParticipants will receive Ritlecitinib 20 mg by mouth once daily (QD).
Ritlecitinib and tolbutamideEXPERIMENTALIn Period 1, participants will be dosed with a single administration of tolbutamide 500 mg tablet on Day 1. Period 1 will be immediately followed by Period 2 with no washout. In Period 2, participants will be dosed with oral 200 mg ritlecitinib QD for 10 days followed by administration of a single dose of 500 mg tolbutamide oral tablet within approximately 5 minutes after administration of a 200 mg dose of ritlecitinib on the morning of Day 10.
Cohort 1EXPERIMENTALSubjects will be dosed with 50 mg Ritlecitinib on Day 1 and followed up till Day 3
Cohort 2EXPERIMENTALSubjects will be dosed with 200 mg Ritlecitinib on Day 1 and followed up till Day 3

Interventions

NameTypeDescription
Ritlecitinib 100 mgDRUG100 mg capsule taken orally once daily
Ritlecitinib 50 mgDRUG50 mg capsule taken orally once daily
PlaceboOTHERCapsule matching either 50mg or 100 mg ritlecitinib capsule taken orally once daily
Placebo - 100 mgDRUGCapsule (to match Ritlecitinib 100 mg)
Placebo - 50 mgDRUGCapsule (to match Ritlecitinib 50 mg)
RitlecitinibDRUGRitlecitinib 50 mg capsule once daily
Ritlecitinib 20 mgDRUGorally administered, Ritlecitinib 20 mg once daily (QD)
TolbutamideDRUGTolbutamide 500 mg provided as one 500 mg oral tablet
Ritlecitinib 200 mgDRUG200 mg single dose
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Eligibility Criteria

Age Range12 Years to N/A
SexALL
Healthy VolunteersNo
Study Sites17

Key Inclusion Criteria * 18 years or older (or the minimum age of consent in accordance with local regulations) at screening. Adolescents (12 to \<18 years of age at screening) are also eligible for this study, but only if permitted by the local IRB/EC and local regulatory health authority (if appl...

Countries:United StatesJapanCanadaChinaCzechiaPolandPuerto RicoSouth KoreaSpainTaiwanUnited KingdomAustraliaBulgariaGermanyMexicoTurkey (Türkiye)BelgiumHungaryItalySlovakiaSouth AfricaGreece
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Recent Changes (Last 90 Days)

HIGHSep 1, 2026NCT07228390Status: RECRUITING → ACTIVE_NOT_RECRUITING
HIGHSep 1, 2026NCT07228390Status: RECRUITING → ACTIVE_NOT_RECRUITING
LOWAug 26, 2026NCT06163326lastUpdatePostDate: changed
LOWAug 26, 2026NCT06163326lastUpdatePostDate: changed
LOWAug 24, 2026NCT07733765Status: NOT_YET_RECRUITING → RECRUITING
LOWAug 24, 2026NCT07733765Status: NOT_YET_RECRUITING → RECRUITING
MEDIUMAug 14, 2026NCT06873945Status: ACTIVE_NOT_RECRUITING → RECRUITING
MEDIUMAug 14, 2026NCT06873945Status: ACTIVE_NOT_RECRUITING → RECRUITING
MEDIUMAug 14, 2026NCT06873945Status: ACTIVE_NOT_RECRUITING → RECRUITING
LOWJul 29, 2026NCT07733765NEW_TRIAL: changed
LOWJul 29, 2026NCT07733765NEW_TRIAL: changed
LOWJul 9, 2026NCT07228390lastUpdatePostDate: changed
LOWJul 9, 2026NCT07228390lastUpdatePostDate: changed
LOWJun 24, 2026NCT06072183lastUpdatePostDate: changed
LOWJun 24, 2026NCT06072183lastUpdatePostDate: changed
LOWJun 18, 2026NCT07219615lastUpdatePostDate: changed
LOWJun 18, 2026NCT07219615lastUpdatePostDate: changed
LOWJun 18, 2026NCT07219615lastUpdatePostDate: changed
LOWJun 18, 2026NCT07219615lastUpdatePostDate: changed

Frequently asked questions about Ritlecitinib

What is Ritlecitinib used for?

Ritlecitinib is an investigational small molecule being studied for dermatologic conditions including stable nonsegmental vitiligo, alopecia areata, and chronic spontaneous urticaria. It is also used in healthy volunteer studies to evaluate pharmacokinetics and drug formulations. The drug is in clinical development and has not been approved for any indication.

What does Ritlecitinib target?

Ritlecitinib is a kinase inhibitor, belonging to the -tinib class of drugs. It works by inhibiting kinase enzymes involved in inflammatory and autoimmune signaling pathways. The specific molecular target is not disclosed in the available data, but its mechanism is consistent with other kinase inhibitors used in dermatology.

Who makes Ritlecitinib?

Ritlecitinib is being developed by Pfizer, Inc., a biopharmaceutical company listed on the New York Stock Exchange under the ticker symbol PFE. Pfizer is conducting clinical trials to evaluate the drug's safety and efficacy across multiple dermatologic indications.

What phase is Ritlecitinib in?

Ritlecitinib is in Phase 3 clinical development for dermatologic indications such as vitiligo and alopecia areata. It is also being studied in Phase 2 trials for chronic spontaneous urticaria and in Phase 1 trials for healthy volunteer pharmacokinetic studies. The drug remains investigational and is not FDA approved.

What clinical trials is Ritlecitinib in?

Ritlecitinib has been studied in four clinical trials. Completed Phase 1 trials include NCT05097716, NCT05852340, and NCT06369454, which evaluated pharmacokinetics and drug formulations in healthy volunteers. An ongoing Phase 2 trial, NCT07219615, is recruiting adults with chronic spontaneous urticaria across multiple countries.

Is Ritlecitinib the same as Ritlecitinib 50 mg or 100 mg?

Ritlecitinib 50 mg and Ritlecitinib 100 mg refer to specific dosage strengths of the same drug, Ritlecitinib. These higher-dose formulations are being evaluated in clinical trials for conditions like vitiligo and alopecia areata. The drug is also referred to simply as Ritlecitinib across different studies.