Concurrent Biologics Registry

Advancing the Science of Concurrent Biologic Therapy

Prospective data on combining biologics remain scarce. The registry aggregates real-world outcomes from published literature and de-identified clinical submissions worldwide, so decisions made one case at a time can draw on the whole record.

Combination Matrix

September 2026

Combination matrix of the 6 most reported biologics in the registry. The most reported pair is Dupilumab plus Omalizumab with 51 patient cases.

Most reported: Dupilumab + Omalizumab (51 cases)

Six most reported biologics shown. Empty cells are combinations awaiting evidence.

Explore the full matrix

178

Patient Cases

52

Combinations

60

Diagnoses

85%

Positive Outcomes

The Problem

A Critical Gap in the Evidence Base

Concurrent biologic use is an increasingly common clinical consideration, yet the data needed to guide it remain scattered.

There is no shared record of how concurrent biologic therapy performs across specialties. Clinicians decide one case at a time, on partial information.

In the clinic

Concurrent therapy is a growing consideration

  • Patients with overlapping immune-mediated conditions
  • Disease refractory to single-agent therapy
  • Decisions spanning gastroenterology, rheumatology, and dermatology

In the literature

The evidence base has not kept pace

  • Isolated case reports and small case series
  • Extrapolation from single-agent data
  • No aggregated record of safety, efficacy, or interactions

The Solution

The First Registry for Concurrent Biologic Therapy

A centralized, curated repository bridging clinical practice and real-world evidence across immune-mediated inflammatory diseases.

  • Centralized evidence

    Cases that would otherwise stay isolated in single publications, or go unreported, are gathered where patterns can be recognized.

  • Multi-center, international

    Published literature and clinical submissions from diverse sites worldwide, reflecting the complexity of real patient populations.

  • Toward consensus

    As the record grows, aggregated data can inform consensus recommendations for concurrent prescribing across specialties.

Isolated case reports and unreported clinical experience are consolidated into one structured registry.

How It Works

A Dual-Source Evidence Model

Published evidence and unpublished clinical experience enter through two complementary pathways and pass a single quality gate.

Source

Published literature

Case reports, case series, and observational studies, extracted into a standardized format.

Source

Clinical submissions

De-identified cases submitted by healthcare professionals through a structured template.

Submit a case
Review

Quality review

Every case is checked for completeness, clinical plausibility, and consistency before inclusion.

Registry

One open record

Aggregated, searchable, and freely accessible to clinicians worldwide.

Clinical scope

What each case records

The registry accepts cases across immune-mediated inflammatory diseases and records the same de-identified variables for each one.

Inclusion criterion

One biologic plus a second biologic or a targeted oral therapy makes one registry case.

At least two concurrent advanced therapies, at least one of which is a biologic. Conventional systemic immunosuppressants are recorded separately as concomitant therapy.

Recorded for every case

  • Demographics

    Age bracket and sex

  • Agents prescribed

    Biologics and targeted oral therapies

  • Primary diagnosis

    Coded to ICD-10

  • Duration

    Length of concurrent therapy

  • Concomitant medications

    Conventional systemic agents

  • Disease activity

    Validated measures, where available

  • Clinical outcome

    On a standardized scale

  • Adverse events

    Observed during treatment

No personally identifiable health information is collected at any stage.

Conditions

Immune-mediated inflammatory diseases across specialties.

Psoriasis & Psoriatic ArthritisAtopic DermatitisHidradenitis SuppurativaChronic Spontaneous UrticariaInflammatory Bowel DiseaseRheumatoid ArthritisAxial SpondyloarthritisSystemic Lupus ErythematosusAutoimmune Blistering Diseases+ many more

Biologics

Any biologic agent, recorded by class or individual molecule.

TNF-alpha InhibitorsIL-17 InhibitorsIL-23 InhibitorsIL-12/23 InhibitorsIL-4/IL-13 Pathway BlockersIL-6 Receptor InhibitorsIL-5 InhibitorsAnti-IgE AgentsB-cell Depleting TherapiesFcRn Inhibitors+ many more

Targeted oral therapies

Targeted synthetic agents and oral targeted peptides, recorded alongside biologics.

JAK InhibitorsTYK2 InhibitorsPDE4 InhibitorsBTK InhibitorsSYK InhibitorsS1P Receptor ModulatorsROCK2 InhibitorsOral IL-23 Receptor Antagonists+ many more

By the Numbers

Registry at a Glance

Real-world evidence from concurrent biologic therapy across published literature and clinical submissions.

178 patient cases from 56 peer-reviewed sources and clinician submissions worldwide. Data current as of September 2026.

0

Patient Cases

From peer-reviewed literature and clinician submissions

0

Unique Combinations

43 biologic pairs, 9 biologic + oral

0%

Positive Outcomes

Of 162 classified outcomes

0%

Adverse Events Reported

25 of 159 cases with reported status

0%

Concomitant Systemic Therapy

34 of 178 cases

Drug Combinations

Therapy Combination Explorer

Patient-level outcome data can be viewed by selecting any combination: biologic pairs by molecule or by drug class, biologic plus targeted oral therapy combinations, or the ranked list of every combination.

Filter the data

Showing 178 of 178 cases.

Diagnosis

Region

Combination

Biologic

Oral therapy

Therapy combination patient counts

n = 152 cases across 43 biologic pairs

Patient case counts for therapy combinations, viewable as a matrix of biologic pairs by molecule or by drug class, as a matrix of biologics against targeted oral therapies, or as a ranked list of every combination. Selecting a populated cell or list entry opens a case-level table below.

Showing 18 of 26 biologics, those with two or more cases.

Dupilumab
Omalizumab
Ustekinumab
Guselkumab
Rituximab
Infliximab
Adalimumab
Risankizumab
Secukinumab
Etanercept
Mepolizumab
Vedolizumab
Golimumab
Tildrakizumab
Evolocumab
Tralokinumab
Anifrolumab
Benralizumab
Dupilumab
Omalizumab
Ustekinumab
Guselkumab
Rituximab
Infliximab
Adalimumab
Risankizumab
Secukinumab
Etanercept
Mepolizumab
Vedolizumab
Golimumab
Tildrakizumab
Evolocumab
Tralokinumab
Anifrolumab
Benralizumab

Fewer
More

26 biologic + targeted oral therapy cases shown separately.

Cohort Composition

Registry Coverage

Where cases are contributed from and which disease combinations drive concurrent biologic therapy.

Geographic distribution

n = 178

Geographic distribution of 178 patient cases by macro region: North America 112 (63%), Europe 39 (22%), Oceania 16 (9%), Asia 10 (6%), South America 1 (1%).

Cases contributed across 5 continents. Selecting a bar filters the data sections by region.

Diagnosis landscape

n = 178

Diagnosis groups across 178 patient cases: Atopic dermatitis (L20) 80, Psoriasis (L40) 80, Chronic urticaria (L50) 48, Inflammatory bowel disease (K50/K51) 25, Asthma (J45) 23, Bullous pemphigoid (L12.0) 15, Granulomatous skin disorders (L92) 4, Hidradenitis suppurativa (L73.2) 3, Rheumatoid arthritis (M05/M06) 2, Systemic lupus erythematosus (M32) 2, Other diagnoses 31.

Groups are not mutually exclusive; a case may carry several diagnoses. Selecting a bar filters the data sections by diagnosis.

Clinical Outcomes

Treatment Response and Demographics

Outcome categorization and demographic distribution across the registry cohort.

Outcome category

n = 178

  • Complete Remission (18)
  • Well Controlled (52)
  • Improvement (67)
  • Mixed (18)
  • No Response (7)
  • Not Reported (16)
Outcome categories across 178 patient cases: Complete Remission 18, Well Controlled 52, Improvement 67, Mixed 18, No Response 7, Not Reported 16.

Age distribution

n = 178

Age distribution of 178 patient cases stacked by sex. 0-9: 1 female, 0 male, 0 not recorded; 10-19: 6 female, 4 male, 1 not recorded; 20-29: 11 female, 6 male, 4 not recorded; 30-39: 16 female, 7 male, 1 not recorded; 40-49: 21 female, 12 male, 3 not recorded; 50-59: 8 female, 21 male, 6 not recorded; 60-69: 15 female, 11 male, 1 not recorded; 70-79: 8 female, 7 male, 0 not recorded; 80+: 2 female, 4 male, 0 not recorded; N/A: 0 female, 0 male, 2 not recorded.

Sex was not recorded for 18 cases, shown in slate.

Treatment Patterns

Duration and Prescribing Trends

Duration of concurrent therapy and prescribing frequency across the cohort.

Treatment duration

n = 178

Treatment duration across 178 patient cases by band: <3m: 12, 3-5m: 37, 6-11m: 46, 12-17m: 26, 18-23m: 11, >24m: 28, N/A: 18.

18 cases without reported duration, shown in slate.

Most prescribed agents

n = 178 cases, two agents each

Most prescribed agents across 178 patient cases, two agents per case, biologics and targeted oral therapies alike. Top agents: Dupilumab (biologic) in 95 cases, Omalizumab (biologic) in 74 cases, Ustekinumab (biologic) in 28 cases, Guselkumab (biologic) in 24 cases, Deucravacitinib (targeted oral therapy) in 22 cases, Rituximab (biologic) in 13 cases, Infliximab (biologic) in 11 cases, Adalimumab (biologic) in 11 cases, Brodalumab (biologic) in 11 cases, Risankizumab (biologic) in 10 cases, plus 20 additional agents.

Safety Data

Adverse Event Profile

Reported adverse events by therapy combination and by sex. All reported events are captured regardless of severity or attribution.

Adverse events by combination

n = 178

Adverse events by therapy combination across 178 patient cases. Dupilumab + Omalizumab (51): 9 with and 42 without an adverse event; Dupilumab + Guselkumab (16): 1 with and 15 without an adverse event; Omalizumab + Rituximab (10): 5 with and 5 without an adverse event; Brodalumab + Deucravacitinib (10): 0 with and 0 without an adverse event, 10 not individually reported; All other combinations (91): 10 with and 72 without an adverse event, 9 not individually reported.

All reported events are shown regardless of severity or attribution; no inference of causality is implied. Combinations with fewer than 10 cases are pooled. 19 cases from series reporting adverse events only at cohort level are shown in slate and excluded from rates.

Adverse events by sex

n = 160 of 178 with recorded sex

Adverse events by sex across 160 patient cases with recorded sex. Female (88): 13 with and 67 without an adverse event, 8 not individually reported; Male (72): 9 with and 52 without an adverse event, 11 not individually reported.

19 cases from series reporting adverse events only at cohort level, shown in slate.

Independent and open access

No industry funding. No paywalls.

The Concurrent Biologics Registry is provided free of charge to clinicians worldwide and operates without pharmaceutical industry funding or compensation.

  • Open access
  • Independent
  • No industry funding

Disclosure statement

Applies to all content

Access to data and visualizationsNo registration, login, or payment required
Free
Pharmaceutical industry fundingNo drug manufacturer supports this work
None
Sponsorship or compensationNo payment from manufacturers or trade groups
None
Industry influence on scope, methodology, or contentEditorial decisions are made independently
None

Trust and transparency

Built on rigor, designed for openness

A freely accessible quality assurance and practice improvement resource that consolidates published and clinician-submitted evidence into a single repository.

De-identified by design

Only aggregate clinical variables are captured: age band, sex, disease category, agents, and outcomes.

Never collected

  • No names
  • No dates of birth
  • No treatment dates
  • No record numbers

Open-access data

The full registry and every visualization are available to anyone, at the point of care.

Access requirements

  • No registration
  • No login
  • No payment

Structured quality review

Every case is reviewed before inclusion so the data stay accurate and clinically credible.

Checked for

  • Completeness
  • Clinical plausibility
  • Consistency

Multi-center collaboration

Cases come from published literature and de-identified submissions contributed by clinicians worldwide.

Sourced from

  • Peer-reviewed literature
  • Clinician submissions
  • International sites

Common Questions

Frequently Asked Questions

Answers to common questions about the Concurrent Biologics Registry, its data, and how to participate.

Concurrent biologic therapy refers to the simultaneous use of two or more advanced therapies in a single patient, at least one of which is a biologic. This typically arises when a patient has multiple immune-mediated conditions, each requiring a distinct agent with a different mechanism of action, or when disease remains refractory to a single agent.
Yes. Targeted synthetic agents such as JAK, TYK2, PDE4, BTK and S1P inhibitors, and oral targeted peptides such as icotrokinra, are recorded alongside biologics and count toward the concurrent therapy requirement. The inclusion criterion is mechanism-based rather than modality-based: an oral agent acting on the IL-23 receptor is pharmacologically comparable to a monoclonal antibody acting on the same pathway, and excluding it would make molecular size a scientific inclusion criterion. Each case must still record at least one biologic. Conventional systemic immunosuppressants such as methotrexate, ciclosporin and systemic corticosteroids are recorded separately as concomitant therapy rather than as advanced therapies.
Validated instruments can be recorded as absolute scores at baseline and follow-up, with a relative follow-up interval. The catalogue covers psoriatic disease (PASI, BSA, sPGA, DAPSA, cDAPSA, MDA, PASDAS, LEI, SPARCC), axial disease (ASDAS, BASDAI, BASFI), rheumatoid arthritis (DAS28, CDAI, SDAI), atopic dermatitis (EASI, SCORAD, POEM, vIGA-AD), urticaria (UAS7, UCT), hidradenitis suppurativa (IHS4, Hurley, HiSCR50), inflammatory bowel disease, autoimmune bullous disease, lupus, and cross-disease measures such as DLQI. Measures relevant to the diagnoses already selected are offered first. Recording them is optional, because retrospective and literature-derived cases frequently lack them, and completeness is reported alongside any derived figure rather than treated as absence. Percentage response criteria such as PASI 90 are deliberately not collected, because a single field cannot distinguish a ninety percent response from an absolute score of nine.
Any licensed healthcare professional managing patients on concurrent advanced therapy. Submissions are accepted from any institution worldwide and undergo structured quality review before inclusion. The registry collects only de-identified, non-identifiable clinical data for quality assurance purposes.
The registry is designed so that personally identifiable health information is never collected. The submission template captures only aggregate clinical variables: age band, biological sex, disease category, biologic and targeted oral agents, duration of therapy, disease activity scores, clinical outcomes, adverse events, care setting, and continent-level geographic region. Follow-up timing is recorded only as a relative interval such as week 24. No patient names, dates of birth, treatment dates, assessment dates, medical record numbers, addresses, or other information that could enable patient re-identification is requested at any stage.
The registry draws from two complementary sources. Published literature: case reports, case series, and observational studies are systematically identified, extracted, and catalogued in a standardized format. Clinician-submitted cases follow a structured de-identified template and undergo quality review before inclusion.
The registry supports clinical decision-making when concurrent biologic therapy is considered, identification of safety signals across biologic combinations not studied in formal trials, and the development of future consensus recommendations for concurrent prescribing. All data and visualizations are freely accessible without registration.

Literature

References

56 peer-reviewed sources, 2005–2026

  1. Response of chronic refractory psoriasis vulgaris with urticaria to combined secukinumab and omalizumab: A case report and review of the literature

    Abdelmaksoud, A., Temiz, S. A., Daye, M., Yavuz, S., Wollina, U., Lotti, T., & Dursun, R.

    Journal of Cosmetic Dermatology202322(4), 1416–1418

  2. Combination treatment with monoclonal antibodies: Dupilumab and ustekinumab for the treatment of severe atopic dermatitis and Crohn disease

    Alegre-Bailo, A., Sánchez-Gilo, A., Gonzalo González, I., & Vicente Martín, F. J.

    Australasian Journal of Dermatology202465(1), 63–66

  3. Dual biologic therapy with Omalizumab and Dupilumab for refractory atopic disease

    Arasu, A., Sharma, N., Yazdabadi, A., & Sladden, M.

    Australasian Journal of Dermatology202263(1), 110–111

  4. Combined biologic therapy for the treatment of psoriasis and psoriatic arthritis: A case report

    Babalola, O., Lakdawala, N., & Strober, B. E.

    JAAD Case Reports20151(1), 3–4

  5. A retrospective review of dupilumab and psoriasis biologic combination therapy

    Barry, K., Zancanaro, P., Casseres, R., Dumont, N., & Rosmarin, D.

    Journal of Dermatological Treatment202132(4), 438–439

  6. Two Track Biologic Therapy for Concurrent Chronic Spontaneous Urticaria and Psoriasis Vulgaris in One Patient

    Benko, M., Hrvatin Stancic, B., & Lunder, T.

    Actas Dermo-Sifiliográficas2022113(10), 995–996

  7. Landmarks for dual biological therapy in inflammatory bowel disease: lesson from two case reports of vedolizumab in combination with ustekinumab

    Biscaglia, G., Piazzolla, M., Cocomazzi, F., Melchionda, G., De Cata, A., Bossa, F., Palmieri, O., & Andriulli, A.

    European Journal of Gastroenterology & Hepatology202032(12), 1579–1582

  8. Navigating the Misdiagnosis of Pityriasis Rubra Pilaris and Successful Treatment With Guselkumab: A Case Report of Dual Biologic Therapy

    Bongfeldt, D., & Martinez-Cabriales, S.

    Cureus202517(12), e98267

  9. Dual biologics therapy in a patient with severe asthma and chronic urticaria: A case report and review of the literature

    Bostan, O. C., Karakaya, G., Kalyoncu, A. F., & Damadoglu, E.

    Journal of Asthma202461(3), 260–264

  10. Dual biologic therapy in a patient with severe asthma and other allergic disorders

    Caskey, J. R., & Kaufman, D.

    BMJ Case Reports202114(5), e242211

  11. Successful treatment of hidradenitis suppurativa in the setting of Crohn disease with combination adalimumab and ustekinumab

    Cline, A., & Pichardo, R. O.

    Dermatology Online Journal201925(9), Article 13030/qt0hw2w4nr

  12. Targeted dual biologic therapy for erythroderma of unknown etiology guided by high-parameter peripheral blood immunophenotyping

    Cornman, H. L., Alphonse, M. P., Dykema, A., Kollhoff, A. L., Lee, K. K., Manjunath, J., Ma, E. Z., Parthasarathy, V., Deng, J., Pritchard, T., Kambala, A., Marani, M., Parr, K. A., Mohammed, J. P., Kwatra, M. M., Bream, J. H., Ho, W. J., & Kwatra, S. G.

    Scientific Reports202515(1), Article 1298

  13. Combination Biologic Treatment of Refractory Psoriasis and Psoriatic Arthritis

    Cuchacovich, R., Garcia-Valladares, I., & Espinoza, L. R.

    The Journal of Rheumatology201239(1), 187–193

  14. Omalizumab and adalimumab: a winning couple

    Diluvio, L., Vollono, L., Zangrilli, A., Manfreda, V., Prete, M. D., Massaro, A., Modica, S., Greco, E., Bianchi, L., & Campione, E.

    Immunotherapy202012(18), 1287–1292

  15. Coesisting inflammatory skin diseases: Tildrakizumab to control psoriasis and omalizumab for urticaria

    Diluvio, L., Pensa, C., Piccolo, A., Lanna, C., Bianchi, L., & Campione, E.

    Dermatologic Therapy202235(4), e15359

  16. The use of dual biologic therapy for the management of recalcitrant psoriasis

    Finnegan, P., Murphy, M., & Bourke, J.

    JAAD Case Reports202447, 93–95

  17. Case Series: Combination of dupilumab and omalizumab as a way to reduce dupilumab-associated adverse events in severe atopic dermatitis

    Fomina, D. S., Mukhina, O. A., Sedova, E. L., Lebedkina, M. S., Bobrikova, E. N., Karaulov, A. V., Lysenko, M. A., & Renz, H.

    Frontiers in Allergy20266, Article 1696897

  18. Combined biologic treatment in patient with chronic spontaneous urticaria and Crohn's disease

    García Martínez, A., Lobato de la Sierra, M. P., & Castro Aguilar-Tablada, T.

    Gastroenterología y Hepatología (English Edition)202548(1), Article 502213

  19. Combined treatment with omalizumab and etanercept in a patient with chronic spontaneous urticaria and rheumatoid arthritis

    Ghazanfar, M. N., & Thomsen, S. F.

    Journal of Dermatological Treatment201930(4), 387–388

  20. Rapid food desensitization supported by omalizumab, with adjunctive dupilumab for type 2 comorbidities: A pediatric case series

    Giavina-Bianchi, P., & Giavina-Bianchi, B.

    World Allergy Organization Journal202619(4), Article 101374

  21. The Combination of Dupilumab with Other Monoclonal Antibodies

    Gisondi, P., Maurelli, M., Costanzo, A., Esposito, M., & Girolomoni, G.

    Dermatology and Therapy202213(1), 7–12

  22. Failure of response to combination therapy of adalimumab and infliximab in a recalcitrant patient of severe psoriasis and major thalassemia: A case report

    Goldust, M., Rahmatpour Rokni, G., Gupta, M., Lotti, T., & Bathaei, M.

    Clinical Case Reports20208(3), 550–552

  23. Safety and efficacy of dual tyrosine kinase 2 inhibitor and monoclonal antibody therapy for psoriasis and psoriatic arthritis

    Guénin, S., Andrews, E., & Lebwohl, M. G.

    British Journal of Dermatology2024190(3), 451–453

  24. Novel combination biologic therapy for recalcitrant psoriasis and psoriatic arthritis in a medically complex patient

    Hanna, S., Youssef, P., & Lowe, P.

    Australasian Journal of Dermatology202263(1), e63–e66

  25. Concurrent use of omalizumab and dupilumab in a 47-year-old woman with chronic spontaneous urticaria and atopic dermatitis

    Holm, J. G., Sørensen, J. A., & Thomsen, S. F.

    International Journal of Dermatology202261(5), e173–e174

  26. The safety and efficacy of dual biological therapy: Dupilumab and fremanezumab

    Honigman, A., Oo, H. P., Macdonell, R., & Kern, J. S.

    Australasian Journal of Dermatology202465(3), e63–e65

  27. Use of dual biologic therapy targeting the Th2 and Th17 axes simultaneously to treat patients with atopic dermatitis and concomitant psoriasis, psoriatic arthritis, or inflammatory bowel disease

    Hren, M. G., Guenin, S., & Khattri, S.

    Journal of the American Academy of Dermatology202491(1), 138–140

  28. Treatment of recalcitrant psoriasis and psoriatic arthritis with a combination of a biologic plus an oral JAK or TYK2 inhibitor: a case series

    Hren, M. G., & Khattri, S.

    Annals of the Rheumatic Diseases202483(10), 1392–1393

  29. Concurrent Atopic Dermatitis and Psoriasis Successfully Treated With Dual Biologic Therapy

    Kaszycki, M. A., Pixley, J. N., & Feldman, S. R.

    Cutis2023112(3), E13–E16

  30. Rituximab and Omalizumab Combination Therapy for Bullous Pemphigoid

    Le, S. T., Herbert, S., Haughton, R., Nava, J., Toussi, A., Ji-Xu, A., & Maverakis, E.

    JAMA Dermatology2024160(1), 107–109

  31. Dual Biological Therapy for Ulcerative Colitis with Intractable Pyoderma Gangrenosum

    Lee, H. C., Kwon, Y., Kim, E. S., Ahn, S., Choe, Y. H., & Kim, M. J.

    Annals of Dermatology202335(Suppl 1), S107–S111

  32. Case Report: Relapsing systemic lupus erythematosus treated with dual rituximab and anifrolumab therapy

    Lee, S., Choi, J., Benitez, S., & Lee, J.

    Frontiers in Medicine202612, Article 1727404

  33. Psoriasis vulgaris flare during efalizumab therapy does not preclude future use: a case series

    Lowes, M. A., Turton, J. A., Krueger, J. G., & Barnetson, R. S.

    BMC Dermatology20055(1), Article 9

  34. Dual Biologic Therapy for Psoriasis in a Patient with Atopic Dermatitis

    Ma, L., Chen, X., Aziz, M. A. A., Chen, A., Cai, T., & Chen, S.

    Psoriasis: Targets and Therapy202515, 159–161

  35. Combination treatment with monoclonal antibodies: Secukinumab, benralizumab and dupilumab for the combined management of psoriasis and severe asthma

    Mahar, P. D., Zubrinich, C. M., Manuelpillai, N., & Foley, P.

    Australasian Journal of Dermatology202162(4), 506–508

  36. Concurrent Use of Anifrolumab and Belimumab in a Patient With Systemic Lupus Erythematosus Presenting With Recurrent Severe Cutaneous Involvement and Lupus Nephritis

    Manjón-Rodríguez, M. D., Borrego-Utiel, F. J., Merino-García, E., Gil-Morillas, A., & Colodro-Ruiz, A.

    Cureus202517(11), e97252

  37. Dual biologics for severe asthma and atopic dermatitis: Synopsis of two cases and literature review

    Matsumoto, T., Sakurai, Y., Tashima, N., Matoba, T., Kaneko, A., Fujiki, T., Kusakabe, Y., Nakayama, E., Tanaka, A., Tashima, M., Yamamoto, N., & Aihara, K.

    Respirology Case Reports202412(1), e01266

  38. Dual Dupilumab and Omalizumab Therapy in Atopic Dermatitis, Chronic Spontaneous Urticaria and Asthma: Real-World Experience From an Eight-Patient Case Series

    McClatchy, J., Morgan, V., Scardamaglia, L., Ramirez, A., & Ross, G.

    Australasian Journal of Dermatology202667(2), 123–125

  39. Pediatric cutaneous Crohn disease: A case series of 89 patients and review

    McKay, G. E., Liu, L., Shaw, K. S., Shakshouk, H., Murphy, M. J., Damsky, W., Ortega-Loayza, A. G., Caplan, A. S., Arkin, L. M., & Shields, B. E.

    Pediatric Dermatology202441(5), 807–813

  40. Dual biologic therapy in a patient with severe psoriasis and psoriatic arthritis, using guselkumab and bimekizumab: A case report and review of the literature

    Muylaert Barrett, B., Music, M., & Yadav, G.

    SAGE Open Medical Case Reports202614, Article 2050313X251411503

  41. Is omalizumab safe and effective in oncological patients?

    Navarro-Triviño, F. J., Mérida-Fernández, C., Linares-Gonzalez, L., & Ruiz-Villaverde, R.

    Dermatologic Therapy201932(6), e13115

  42. Off-Label Uses of Deucravacitinib for Inflammatory Skin Conditions: Cases and Literature Review

    Nigro, A., Silva, I. C., Gerstein, B., Dayanan, J., & Khattri, S.

    Case Reports in Dermatological Medicine20262026(1), Article 9941426

  43. An Unusual Case of Psoriasiform Dermatitis Treated With Dual Biologic Therapy and Literature Review

    Nong, Y., Marson, J. W., Derrick, K., Heilman, E., Schneider, J., Feig, J. L., & Siegel, D. M.

    Journal of Drugs in Dermatology202524(2), 207–211

  44. Combination of Biological Agents in Moderate to Severe Pediatric Inflammatory Bowel Disease: A Case Series and Review of the Literature

    Olbjørn, C., Rove, J. B., & Jahnsen, J.

    Pediatric Drugs202022(4), 409–416

  45. Combined Biologic Therapy in 2 Patients With Severe Psoriasis and Severe Atopic Dermatitis

    Pascual Ares, M., Orbea Sopeña, A., Aramburu González, A., & Gardeazábal García, J.

    Actas Dermo-Sifiliográficas2024115(5), T527–T529

  46. Combining Biologics Targeting Eosinophils (IL-5/IL-5R), IgE, and IL-4/IL-13 in Allergic and Inflammatory Diseases

    Pitlick, M. M., & Pongdee, T.

    World Allergy Organization Journal202215(11), Article 100707

  47. Case report: Severe chronic spontaneous urticaria successfully treated with omalizumab and dupilumab

    Puxkandl, V., Hoetzenecker, W., & Altrichter, S.

    Allergologie Select20237(1), 17–19

  48. Combination therapy including dupilumab, omalizumab, and mycophenolate mofetil for refractory bullous pemphigoid

    Ratnarajah, K., Arès, S., Kechichian, E., & Lucena Fernandes, C.

    JAAD Case Reports202565, 201–205

  49. Case Report: Combination of Omalizumab and Dupilumab for Recalcitrant Bullous Pemphigoid

    Seyed Jafari, S. M., Feldmeyer, L., Bossart, S., Simon, D., Schlapbach, C., & Borradori, L.

    Frontiers in Immunology202111, Article 611549

  50. Combined use of Omalizumab and dupilumab: safety and efficacy data from a large academic center

    Silva, I. C., Daher, R., & Khattri, S.

    Archives of Dermatological Research2025317(1), Article 674

  51. Recalcitrant erythrodermic ichthyosis with atopic dermatitis successfully treated with Dupilumab in combination with Guselkumab

    Steinhoff, M., Al-Marri, F., Al Chalabi, R., Gieler, U., & Buddenkotte, J.

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  52. Dual Biologic Therapy With Dupilumab and Risankizumab for Coexistent Prurigo Nodularis and Psoriasis

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    International Journal of Dermatology202665(4), 901–903

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    Thibodeaux, Q., Ly, K., Reddy, V., Smith, M. P., & Liao, W.

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  54. Combination biologic therapy for the treatment of severe palmoplantar pustulosis

    Torre, K. M., & Payette, M. J.

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  55. Severe case of bullous pemphigoid associated with nivolumab responsive to combination therapy with dupilumab and omalizumab

    Victory, L., Murray, G., Quigley, C., Bowe, S., Feighery, C., Fortune, A., & McDonald, I.

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  56. Golimumab in Children with Chronic Recurrent Multifocal Osteomyelitis: A Case Series and Review of the Literature

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    Paediatric Drugs202325(5), 603–611

Contribute

Contribute to the Registry

Clinicians managing patients on concurrent biologic therapy are invited to contribute data. Each submission strengthens the evidence base for concurrent biologic prescribing.

What to Submit

  • De-identified patient demographics
  • Biologic agents and concurrent therapy details
  • Primary diagnosis (ICD-10 coded)
  • Duration and clinical outcomes
  • Adverse events observed during treatment