A Phase 1/2 Study of Oral LOXO-292 in Patients
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- STATUS
- Recruiting
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- participants needed
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Summary
LOXO-292 is a highly potent and specific inhibitor of the RET RTK, with minimal inhibition of other kinase and non-kinase targets, and therefore may be of benefit to patients with tumors (such as NSCLC, MTC, PTC, and colon or breast carcinomas) that harbor RET alterations and/or depend on RET activation. This Phase 1/2 study of LOXO-292 is required to understand the PK, safety, and maximum tolerated dose (MTD) for LOXO-292 in patients and to permit the preliminary assessment of efficacy.
Details
| Condition | TBD |
|---|---|
| Age | 99years or below |
| Clinical Study Identifier | 03157128 |
| Last Modified on | 19 February 2024 |
Eligibility
How to participate?
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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