ClinicalTrials.gg
AvailableNCT04776694Updated Sep 1, 2026

Compassionate Use or Expanded Access of Dupilumab

An expanded access record providing Dupilumab in Type 2 Inflammatory Disorders, sponsored by Regeneron Pharmaceuticals. Available. Open to participants aged 6 Months and older. Per ClinicalTrials.gov, last updated 2026-09-01.

Sponsored by Regeneron Pharmaceuticals · Expanded access

Study type
Expanded access
Access type
Individual patients · Treatment IND/protocol
Ages
6 Months and older
Sex
All
01

Study summary

Provide Compassionate Use or Expanded Access of Dupilumab

Read the detailed description

Compassionate Use or Expanded Access requests are only being considered in response to Individual Patient or Treatment Investigational New Drug (IND) applications. Availability will depend on location.

02

Conditions studied

  • Type 2 Inflammatory Disorders

Keywords

  • Allergies
  • Hand and Foot Dermatits
  • Eosinophilic Esophagitis (EoE) - Pediatrics
  • Hailey-Hailey Disease
  • Nasal Polysposis (NP)
  • Idiopathic Urticaria
  • Dermal Hypersensitivity Reaction
  • Eosinophilic Gastrointestinal Disease (EGID)
  • Actinic Prurigo
  • Eosinophilic Cystitis
  • Allergic Rhinitis with Nasal Polyposis
  • Epidermolysis Bullousa Simplex (EBS)
  • Chronic Spontaneous Urticaria (CSU)
  • Cicatricial Pemphigoid
  • Pemphigus Foliaceus
  • Disseminated Coccidiomycosis
  • Topical steroid withdrawal syndrome
  • Middle ear disease
  • Eosinophilic Enterocolitis
03

In context

Hypersensitivity

1,055 studies on the registry are indexed under Hypersensitivity; 149 are open to participants now.

Browse Hypersensitivity studies →

Lead sponsor

Regeneron Pharmaceuticals is the lead sponsor of 411 studies on the registry; 90 are open to participants now.

Of its 125 completed or terminated interventional studies of FDA-regulated products, 79 (63%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
6 Months and older
Sexes eligible
All

Eligibility criteria

Eligibility will be determined during the application review process.

05

Access details

Study type
Expanded access
Access type
Individual patients · Treatment IND/protocol

Available treatment

  • To be provided by Regeneron

    Also known as: REGN668, DUPIXENT®, SAR231893

06

Where to request access

No study locations are listed for this record.

07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 1, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT04776694
Responsible party
Sponsor
First posted
Mar 2, 2021
Last update
Sep 1, 2026

Study contacts

Requests must be initiated by a treating physician. Physicians should contact
Contact
compassionateuserequests@regeneron.com
844-734-6643
View the source record on ClinicalTrials.gov ↗

Requesting access

Expanded access is arranged between your doctor and the company. Ask your care team to contact the provider listed on this record.

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