Phase 1
N=54
A Study for Participants With Advanced Cancer
Advanced Cancer · Metastatic Cancer
Bottom Line
View on ClinicalTrials.gov: NCT01214629 ↗Enrolled (actual)
54
Serious AEs
48.2%
Results posted
Aug 2018
Primary outcome: Primary: Recommended Dose for Phase 2 Studies — 4.0; 6.0 mg/m²/day
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 1
- Interventions
- LY2523355 (Drug); pegfilgrastim (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Eli Lilly and Company
- Primary completion
- May 2012
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Recommended Dose for Phase 2 Studies |
4.0; 6.0 | — |
| SECONDARY Number of Participants With Clinically Significant Effects |
0; 0; 0; 1; 0; 5 | — |
| SECONDARY Pharmacokinetics: Maximum Plasma Concentration (Cmax) of LY2523355 Following A Single Dose |
32.6; 61.7; 120; 127; 168; 222 | — |
| SECONDARY Pharmacokinetics: Plasma Cmax of LY2523355 Following Multiple Doses |
29.8; 73.6; 126; 129; 193; 231 | — |
| SECONDARY Pharmacokinetics: Area Under the Plasma Concentration-Time Curve From Time Zero to Infinity [AUC(0-∞)] of LY2523355 Following A Single Dose |
81.8; 159; 324; 379; 443; 642 | — |
| SECONDARY Pharmacokinetics: AUC(0-∞) of LY2523355 Following Multiple Doses |
109; 220; 484; 593; 649; 1090 | — |
| SECONDARY Number of Participants With Tumor Response |
0; 0; 0; 0; 0; 0 | — |
Summary
This study is being conducted to determine the safety of LY2523355 for the treatment of advanced and/or metastatic cancer (including Non-Hodgkin's lymphoma).
Eligibility Criteria
Inclusion Criteria
- Have a diagnosis of advanced and/or metastatic cancer (solid tumors or Non-Hodgkin's lymphoma) that is refractory to standard therapy or for which no proven effective therapy exists. Participants entering Part B of the study must also have a tumor that is safely amenable to serial biopsies
- Have the presence of measurable or nonmeasurable disease as defined by the Response Evaluation Criteria in Solid Tumors (RECIST, Therasse et al. 2000) or Revised International Working Group Lymphoma Response Criteria (Cheson et al. 2007)
- Have a performance status of 0 or 1 on the Eastern Cooperative Oncology Group (ECOG) scale
- Have discontinued all previous therapies for cancer, including chemotherapy, radiotherapy, cancer-related hormonal therapy, or other investigational therapy for at least 28 days (6 weeks for mitomycin-C or nitrosoureas) prior to study enrollment
- Males and females with reproductive potential must agree to use medically approved contraceptive precautions during the trial and for 3 months following the last dose of study drug
- Females with child bearing potential must have had a negative urine or serum pregnancy test less than or equal to 7 days prior to the first dose of study drug
- Have an estimated life expectancy of greater than or equal to 12 weeks
Exclusion Criteria
- Have symptomatic, untreated or uncontrolled central nervous system (CNS) metastases. Participants with treated CNS metastases are eligible provided their disease is radiographically stable, asymptomatic, and they are not currently receiving corticosteroids and/or anticonvulsants. Screening of asymptomatic participants without history of CNS metastases is not required
- Have current acute or chronic leukemia
- Have had an autologous or allogenic bone marrow transplant
- Have the following conduction abnormalities: PR >250 milliseconds (msec), second degree or complete atrioventricular (AV) block, intraventricular conduction delay (IVCD) with QRS ≥120 msec, left branch bundle block (LBBB), right branch bundle block (RBBB), Wolf-Parkinson- White syndrome (WPW), left anterior fascicular block (LAFB), left posterior fascicular block (LPFB), or other conduction abnormality that in the opinion of the investigator would preclude safe participation in this study.
- Females who are pregnant or lactating
- Known hypersensitivity to pegfilgrastim or filgrastim
Data sourced from ClinicalTrials.gov (NCT01214629). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.