Summary

Eligibility
for people ages 18 years and up (full criteria)
Location
at Los Angeles, California and other locations
Dates
study started
completion around
Principal Investigator
by Saeed Sadeghi, MD
Headshot of Saeed Sadeghi
Saeed Sadeghi

Description

Summary

This is a phase I, First-in-Human (FIH), open-label study to evaluate the safety, tolerability, pharmacokinetic (PK) profile, and preliminary efficacy of RGT-419B administered orally as monotherapy OR in combination with Hormonal Therapy in subjects with HR+, HER2- locally advanced and unresectable (Stage III) or metastatic (Stage IV) breast cancer whose disease has progressed during prior therapy with an approved CDK4/6i plus hormonal therapy.

Official Title

First-in-Human, Escalating Oral Dose Study of RGT-419B Given Alone and With Endocrine Therapy in Subjects With Hormone Receptor Positive, Human Epidermal Growth Factor Receptor 2 Negative Advanced/Metastatic Breast Cancer

Keywords

Breast Cancer, Breast Neoplasms, RGT-419B, RGT-419B in combination with hormonal therapy

Eligibility

You can join if…

Open to people ages 18 years and up

  1. Male or female >/= 18 years old
  2. ECOG Performance Status 0 to 1
  3. Subjects must have histologically or cytologically confirmed diagnosis of ER+, HER2- ABC consistent with ASCO CAP guidelines that is locally advanced and unresectable (Stage III) or metastatic (Stage IV) BC.
  4. Measurable AND evaluable lesions at baseline per RECIST v1.1.
  5. Eligible subjects must meet all of the following criteria:
    • Progression after receiving 1 line of prior cyclin-dependent kinase 4 and 6 inhibitor (CDK4/6i) therapy combined with HT in the MBC setting (up to 1 additional line of CDK4/6i is permitted in the post-surgical adjuvant setting);
      • Subjects must have received therapy for ≥3 months in the MBC setting, or for ≥6 months in the adjuvant setting, prior to progression
    • Progression after ≤3 lines of prior HT therapy (regardless of whether it is HT alone or in combination with other therapies)
      • Prior HT combination agents, including SERD, SERM or AI, must have received formal approval by regulatory agency.
    • ≤ 1 prior line of chemotherapy in the metastatic setting
  6. Adequate organ function
  7. Ability to understand and the willingness to sign a written informed consent document

You CAN'T join if...

  1. Presence of visceral metastases with severe organ dysfunction as evidence by signs and symptoms, laboratory studies, lymphangitic spread and/or rapid progression of disease
  2. Pregnant or planning to become pregnant
  3. Prior irradiation to >25% of the bone marrow and/or inadequate bone marrow function or evidence of clinically significant end-organ damage
  4. Major surgery, chemotherapy, targeted therapy, experimental agents, or radiation within 14-28 days prior to Cycle 1, Day 1
  5. Active, serious medical condition that is not well controlled with locally approved medications allowed by the protocol
  6. History of allergic reactions attributed to compounds of similar chemical or biologic composition to the drugs used in the study

Locations

  • University California, Los Angeles accepting new patients
    Los Angeles California 90404 United States
  • University of California, San Diego accepting new patients
    La Jolla California 92037 United States

Lead Scientist at UCLA

  • Saeed Sadeghi, MD
    HS Clinical Professor, Medicine. Authored (or co-authored) 24 research publications

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Regor Pharmaceuticals Inc.
Links
Sign up for this study
ID
NCT05304962
Phase
Phase 1 Breast Cancer Research Study
Study Type
Interventional
Participants
Expecting 64 study participants
Last Updated