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Clinical Trial Details — Status: No longer available

Administrative data

NCT number NCT03052569
Other study ID # RXDX-105 - EAP
Secondary ID
Status No longer available
Phase
First received
Last updated

Study information

Verified date April 2019
Source Hoffmann-La Roche
Contact n/a
Is FDA regulated No
Health authority
Study type Expanded Access

Clinical Trial Summary

Expanded access to RXDX-105 will be given to patients with cancers harboring RET alterations who have not received TKIs that target RET alterations, who do not qualify for participation in, or who are otherwise unable to access, an ongoing clinical trial for RXDX-105.


Recruitment information / eligibility

Status No longer available
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Diagnosis of advanced cancer with RET alterations

- Unable to participate in an ongoing RXDX-105 clinical trial

- Willing and able to provide written, signed informed consent

- Medically suitable for treatment with RXDX-105

Exclusion Criteria:

- Prior treatment with a TKI that has activity against RET alterations

- Currently enrolled in an ongoing clinical study with any other investigational agent

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
RXDX-105
Oral Capsules

Locations

Country Name City State
United States Www.Ignyta.Com San Diego California

Sponsors (1)

Lead Sponsor Collaborator
Hoffmann-La Roche

Country where clinical trial is conducted

United States,