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Clinical Trial Summary

An open-label, dose-escalation (Part 1), dose-expansion (Part 2) study to assess the safety, pharmacokinetics (PK), and preliminary efficacy of ABBV-155 alone and in combination with paclitaxel or docetaxel. In Part 1 (dose escalation), participants will receive escalating doses of ABBV-155 monotherapy (Part 1a) or ABBV-155 in combination with paclitaxel or docetaxel (Part 1b). In Part 2 (dose expansion), participants will receive ABBV-155 monotherapy or in combination therapy. The ABBV-155 monotherapy cohort will enroll participants with relapsed or refractory (R/R) small cell lung cancer (SCLC) (Part 2a); the ABBV-155 plus a taxane (paclitaxel or docetaxel) combination cohort will enroll participants with R/R non-small cell lung cancer (NSCLC) and breast cancer (Part 2b).


Clinical Trial Description

The Escalation cohorts (Part 1) have been completed. The expansion cohorts (Part 2) are open to enrollment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03595059
Study type Interventional
Source AbbVie
Contact
Status Active, not recruiting
Phase Phase 1
Start date July 13, 2018
Completion date December 31, 2024

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