Mode
Text Size
Log in / Sign up
Phase 2 N=169 Treatment

A Study of Prexasertib (LY2606368) in Platinum-Resistant or Refractory Recurrent Ovarian Cancer

Ovarian Cancer

Enrolled (actual)
169
Serious AEs
43.8%
Results posted
Jun 2020
Primary outcome: Primary: Percentage of Participants Who Achieve Complete Response (CR) or Partial Response (PR): Overall Response Rate (ORR) — 11.3; 13.0; 12.2; 6.9 Percentage of Participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Prexasertib (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
Female
Sponsor
Eli Lilly and Company
Primary completion
Jun 2019

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Participants Who Achieve Complete Response (CR) or Partial Response (PR): Overall Response Rate (ORR)
11.3; 13.0; 12.2; 6.9
SECONDARY
Pharmacokinetics (PK): Maximum Plasma Concentration (Cmax) of Prexasertib
668; 718; 678; 672
SECONDARY
Disease Control Rate (DCR): Percentage of Participants With a Best Overall Response of CR, PR, or Stable Disease (SD) for at Least 4 Months
45.3; 32.6; 31.7; 31.0
SECONDARY
Duration of Response
8.57; 3.84; 5.55; 5.31
SECONDARY
Percentage of Participants With at Least a 50% Reduction in CA-125 Levels From Baseline
39.6; 34.8; 17.1; 37.9
SECONDARY
Progression-Free Survival
3.91; 3.71; 3.58; 3.71
SECONDARY
Overall Survival
13.04; 14.32; 11.14; 8.18

Summary

The purpose of this study is to evaluate the efficacy and safety of prexasertib in women with platinum-resistant or refractory recurrent ovarian cancer.

Eligibility Criteria

Inclusion Criteria

  • Women who have high-grade serous ovarian, primary peritoneal or fallopian tube cancer.
  • Cohorts 1 to 3: Have platinum-resistant disease and have documented test results assessing alterations in the BRCA1 and BRCA2 genes prior to receiving study treatment.
  • Cohort 1: Are BRCA negative and have received 3 or more prior lines of therapy.
  • Cohort 2: Are BRCA negative and have received less than 3 prior lines of therapy.
  • Cohort 3: Are BRCA positive and have previously received a PARP.
  • Cohort 4: Have primary platinum refractory disease.
  • Have adequate organ function.
  • Must be able and willing to undergo mandatory tumor biopsy.

Exclusion Criteria

  • Cohorts 1-3: Have previously received all of the following agents at any time in the platinum-resistant setting: gemcitabine, pegylated liposomal doxorubicin, and paclitaxel.
  • Have known central nervous system malignancy or metastasis.
  • Have previously participated in any study involving a checkpoint kinase 1 inhibitor or have hypersensitivity to the study drug or excipients.
  • Have at least one of the following:
  • history of abdominal fistula or gastrointestinal perforation
  • intra-abdominal abscess within last 3 months prior to the first dose of study drug
  • a radiographically confirmed bowel obstruction within 3 months prior to the first dose of study drug
  • Have a symptomatic human immunodeficiency virus infection or symptomatic activated/reactivated hepatitis A, B, or C (screening is not required).
  • Have a serious cardiac condition.
  • Have a history of prior radiotherapy to the whole pelvis.
  • Have chronic daily treatment with corticosteroids, excluding inhaled or topical steroids.
  • Have known factors that may increase the risk of infection while on study drug treatment. These may include, but are not limited to, an indwelling peritoneal catheter or open wounds. Catheters for vascular access are permitted.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03414047). 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.

Back to search