A Study of LOXO-783 in Patients With Breast Cancer/Other Solid Tumors

Phase
Recruitment status
Participants
Lead sponsor
Eli Lilly and Company
Start date
Number of sites

Summary
The main purpose of this study is to learn more about the safety, side effects, and effectiveness of LOXO-783. LOXO-783 may be used to treat breast cancer and other solid tumors that have a change in a particular gene (known as the PIK3CA gene). Participation could last up to 36 months (3 years) and possibly longer if the disease does not get worse.
Acronym
Short title
A Study of LOXO-783 in Patients With Breast Cancer/Other Solid Tumors
Official title
A Study of LOXO-783 Administered as Monotherapy and in Combination With Anticancer Therapies for Patients With Advanced Breast Cancer and Other Solid Tumors With a PIK3CA H1047R Mutation

Control arm
Registry reports results
Listing at source
Recruitment status
Phase
Study type
Interventional

Completion date
First posted
Registry last updated
Primary completion date
Start date

Participants
Participant count basis
Planned participants
Protocol amendments
Number of sites

Data monitoring committee
Registry sponsor category
Lead sponsor
Eli Lilly and Company
Source registry
ClinicalTrials.gov

Registry ID
ClinicalTrials.gov ID
Registry record
Open registry record

Allocation
Not randomised
Model
Sequential
Purpose
Treatment
Masking
No masking
Sources for study design

  1. Phase 1 a: To determine the maximum tolerated dose/recommended phase 2 dose (MTD/RP2D) of LOXO-783: Number of patients with dose-limiting toxicities (DLTs)

    Timeframe: During the first 28-day cycle of LOXO-783 treatment

    Number of patients with DLTs

  2. Phase 1 a: To determine the MTD/RP2D of LOXO-783: Number of patients with DLT-equivalent toxicities

    Timeframe: During the first 28-day cycle of LOXO-783 treatment

    Number of patients with DLT-equivalent toxicities

  1. To assess the pharmacokinetics (PK) of LOXO-783: Area under the concentration versus time curve (AUC)

    Timeframe: Up to 2 months

    PK of LOXO-783: AUC

  2. To assess the PK of LOXO-783: Maximum drug concentration (Cmax)

    Timeframe: Up to 2 months

    PK of LOXO-783: Cmax

  3. To evaluate the preliminary antitumor activity of LOXO-783: Overall response rate (ORR)

    Timeframe: Up to approximately 36 months or 3 years

    ORR per investigator assessed Response Evaluation Criteria in Solid Tumors, version 1.1 (RECIST 1.1)

  4. To evaluate the preliminary antitumor activity of LOXO-783: Best overall response (BOR)

    Timeframe: Up to approximately 36 months or 3 years

    BOR per investigator assessed RECIST 1.1

  5. To evaluate the preliminary antitumor activity of LOXO-783: Duration of response (DOR)

    Timeframe: Up to approximately 36 months or 3 years

    DOR per investigator assessed RECIST 1.1

  6. To evaluate the preliminary antitumor activity of LOXO-783: Disease control rate (DCR)

    Timeframe: Up to approximately 36 months or 3 years

    DCR per investigator assessed RECIST 1.1

  7. To evaluate the preliminary antitumor activity of LOXO-783: Clinical benefit rate (CBR)

    Timeframe: Up to approximately 36 months or 3 years

    CBR per investigator assessed RECIST 1.1

  8. To evaluate the preliminary antitumor activity of LOXO-783: Time to response (TTR)

    Timeframe: Up to approximately 36 months or 3 years

    TTR per investigator assessed RECIST 1.1

  9. To evaluate the preliminary antitumor activity of LOXO-783: Progression free survival (PFS)

    Timeframe: Up to approximately 36 months or 3 years

    PFS per investigator assessed RECIST 1.1

  10. To evaluate the preliminary antitumor activity of LOXO-783: Overall survival (OS)

    Timeframe: Up to approximately 36 months or 3 years

    OS per investigator assessed RECIST 1.1

Sources for outcomes

Sex
All
Age groups
Adults, Older adults
Minimum age
18 Years
Healthy volunteers
No

  • Have advanced breast cancer or another solid tumor with the presence of a phosphatidylinositol 3-kinase catalytic subunit alpha (PIK3CA) H1047R mutation (or other Sponsor and safety review committee (SRC)-approved, activating PIK3CA mutations other than H1047R mutation)

  • Have adequate archival tumor tissue sample available or be approved by the Sponsor for enrollment if no tumor sample is available.

  • Have stopped all cancer treatment and have recovered from the major side effects

  • Have adequate organ function, as measured by blood tests

  • Have a performance status of 0 or 1 on the Eastern Cooperative Oncology Group (ECOG) scale

  • Patients must have

    • Measurable disease

      --- Patients with non-breast tumor types must have at least 1 measurable lesion

    • Non-measurable bone disease (at least 1 bone lesion in breast cancer patients only)

  • For patients with an estrogen receptor (ER)+ breast cancer diagnosis:

    • If female, must be postmenopausal
    • If male, must agree to use hormone suppression
  • Phase 1a:

    -- Dose escalation and backfill patients:

    • Advanced solid tumor
    • Patients may have had up to 5 prior regimens for advanced disease
  • Phase 1b:

    • Part A:

      • ER+/human epidermal growth factor receptor 2 (HER2)- advanced breast cancer
      • Patients may have had up to 5 prior regimens for advanced disease ---- Prior cyclin dependent kinase (CDK)4/6 inhibitor therapy required
    • Part B:

      • ER+/HER2- advanced breast cancer
      • Patients may have had up to 2 prior regimens for advanced disease.
    • Part C:

      • ER+/HER2- advanced breast cancer

      • Patients may have had up to 5 prior regimens for advanced disease.

        ---- Prior CDK4/6 inhibitor therapy required.

      • Have a diagnosis of diabetes mellitus Type 2

    • Part D:

      • Advanced breast cancer
      • Patients may have had up to 5 prior regimens for advanced disease.
    • Part E:

      • Advanced solid tumor
      • Patients may have had up to 3 prior regimens for advanced disease advanced disease
    • Part F:

      • ER+/HER2- advanced breast cancer

      • Patients may have had up to 5 prior regimens for advanced disease

        • Prior cyclin dependent kinase (CDK)4/6 inhibitor therapy required

  • Medical Conditions

    • Colorectal cancer

    • Endometrial cancers with specific concurrent oncogenic alterations

    • A history of known active or suspected

      • Diabetes mellitus Type 1 or
      • Diabetes mellitus Type 2 requiring antidiabetic medication (Phase 1a and all parts of Phase 1b except Part C).
      • Serious concomitant systemic disorder
  • Known or suspected history of untreated or uncontrolled central nervous system (CNS) involvement.

  • Active uncontrolled systemic bacterial, viral, fungal, or parasitic infection, or other clinically significant active disease process

  • Prior exposure to phosphatidylinositol 3-kinase/protein kinase B/mammalian target of rapamycin (PI3K/AKT/mTOR) inhibitor(s), except in certain circumstances

Sources for eligibility

  • Mayo Clinic of ScottsdaleScottsdale, United StatesNot yet recruiting
  • UCLA Medical CenterLos Angeles, United StatesCompleted
  • UCSF Medical Center at Mission BaySan Francisco, United StatesRecruiting
  • Stanford University HospitalStanford, United StatesRecruiting
  • Mayo ClinicJacksonville, United StatesNot yet recruiting
  • Winship Cancer Center Emory UniversityAtlanta, United StatesCompleted
  • Massachusetts General HospitalBoston, United StatesCompleted
  • Dana-Farber Cancer InstituteBoston, United StatesNot yet recruiting
  • Mayo ClinicRochester, United StatesRecruiting
  • Washington University Medical SchoolSt Louis, United StatesNot yet recruiting
  • Memorial Sloan Kettering Cancer CenterNew York, United StatesCompleted
  • Wilmot Cancer InstituteRochester, United StatesNot yet recruiting
  • Tennessee Oncology PLLCNashville, United StatesCompleted
  • Texas Oncology-Baylor Charles A. Sammons Cancer CenterDallas, United StatesNot yet recruiting
  • UT Southwestern Medical CenterDallas, United StatesRecruiting
  • University of Texas MD Anderson Cancer CenterHouston, United StatesNot yet recruiting
  • South Texas Accelerated Research Therapeutics (START)San Antonio, United StatesNot yet recruiting
  • Cancer Research SAAdelaide, AustraliaNot yet recruiting
  • Peter Maccallum Cancer Institute ErbEast Melbourne, AustraliaNot yet recruiting
  • St Vincent's HospitalSydney, AustraliaNot yet recruiting
  • Institut Jules BordetAnderlecht, BelgiumNot yet recruiting
  • Universitaire Ziekenhuizen Leuven - Campus GasthuisbergLeuven, BelgiumNot yet recruiting
  • Princess Margaret Hospital (Hong Kong)Toronto, CanadaRecruiting
  • BC Cancer VancouverVancouver, CanadaRecruiting
  • Beijing Cancer hospitalBeijing, ChinaNot yet recruiting

And 25 more, listed on the interactive page.

Sources for sites

  • 2022-000175-40
  • J4C-OX-JZUA
Sources for references

Related records

Drugs (7)

Lead sponsors (1)

Conditions (2)

Targets (19)