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Expanded Access to ABT-414

Expanded Access to ABT-414

Status
NO_LONGER_AVAILABLE
Phases
Unknown
Study type
Expanded Access
Source
ClinicalTrials.gov
Registry ID
NCT03123952
Enrollment
Unknown
Registered
2017-04-21
Start date
Unknown
Completion date
Unknown
Last updated
2019-07-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Glioblastoma or Solid Tumors, Epidermal Growth Factor Receptor (EGFR) Diagnosis

Keywords

Expanded Access, Pre-approval Access, Compassionate Use, Special Access Program, Named Patient Basis, Special Access Scheme

Brief summary

This is an expanded access program (EAP) for eligible participants. This program is designed to provide access to ABT-414 prior to approval by the local regulatory agency. Availability will depend on territory eligibility. Participating sites will be added as they apply for and are approved for the EAP. A medical doctor must decide whether the potential benefit outweighs the risk of receiving an investigational therapy based on the individual patient's medical history and program eligibility criteria.

Interventions

ABT-414 will be administered by intravenous infusion

Sponsors

AbbVie
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Participant must have epidermal growth factor receptor (EGFR) amplification or EGFRvIII mutation. * Health Care Provider (HCP) must have prior clinical trial experience with ABT-414. * The participant must not be eligible for an ABT-414 clinical trial. * Pediatric participants may be evaluated on a case by case basis.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026