Overview
Study to Test the Safety and Tolerability of PF-07220060 in Participants With Advance Solid Tumors
Status:
Recruiting
Recruiting
Trial end date:
2025-04-08
2025-04-08
Target enrollment:
0
0
Participant gender:
All
All
Summary
This is a Phase 1, open label, multicenter, nonrandomized, multiple dose, safety, tolerability, pharmacokinetic and pharmacodynamic study of PF-07220060 administered as a single agent and then in combination with endocrine therapy. In Part 1A, single escalating doses of PF-07220060 alone will be administered to determine the maximum tolerated dose (MTD) and select the recommended phase 2 dose (RP2D). In Part 1B and Part 1C, PF-07220060 will be administered in combination with 1 of 2 endocrine therapies (letrozole and fulvestrant, respectively). In Part 1D, food effect assessment of PF-07220060 at the RP2D dose level from the Part 1A will be conducted. Part 1B and Part 1C may commence at MTD or before reaching the MTD at a dose level in Part 1A. Part 2B and Part 2C are expansion for combination therapy of PF-07220060 with letrozole and fulvestrant, respectively.Phase:
Phase 1Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
PfizerTreatments:
Fulvestrant
Letrozole
Criteria
Inclusion Criteria- Part 1: Breast Cancer (BC)
- Refractory Hormone Receptor Positive (HR+), Human Epidermal Growth Factor
Receptor 2 Negative (HER2-) BC
- Part 1A/Part 1D also include: Refractory HR-positive/HER2-positive BC
- Part 1: Tumors other than BC (Part 1A/Part 1D): NSCLC, prostate, CRC, liposarcoma, or
tumors with previously confirmed CDK4 or CCND1 amplification according to local
standard tests
- Part 2:
- HR-positive/HER2-negative BC
- Patients who are either postmenopausal women or pre/peri-menopausal (Part 2C
only)
- Lesion:
- Part 1: evaluable lesion (including skin or bone lesion only)
- Part 2: measurable lesion per RECIST v1.1
- Prior systemic Treatment
- Part 1: HR-positive/HER2-negative BC
- At least 1 line of SOC, including CD4/6 inhibitor therapy for advanced or
metastatic disease, or if CDK4/6 inhibitors are not considered appropriate
in the opinion of the investigator
- At least 1 line of anti-endocrine in countries without CDK4/6 inhibitor
approval or reimbursement, for advanced or metastatic disease
- HR-positive/HER2-positive BC (Parts 1A/1D): at least 1 prior treatment of
approved HER2 targeting therapy
- Tumors other than BC (Parts 1A/1D): tumor that is resistant to at least 2
lines of SOC for advanced or recurrent disease or for which no standard
therapy is available
- Part 2B: participants who have not received any prior systemic anti-cancer
therapies for advanced/metastatic BC
- Part 2C:
- Progressed during treatment or within 12 months of completion of adjuvant
therapy with an aromatase inhibitor if postmenopausal, or tamoxifen if pre
or perimenopausal, or
- Progressed while on or within 1 month after the endo the prior aromatase
inhibitor therapy for advanced/metastatic BC if postmenopausal or prior
endocrine treatment for advanced/metastatic BC if pre or perimenopausal
- One previous line of chemotherapy for advanced/metastatic disease is allowed
in addition to endocrine therapy
General Inclusion Criteria
- All participants must be refractory to or intolerant of existing therapies known to
provide clinical benefit for their condition.
- Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) 0 or 1
- Adequate renal, liver, and bone marrow function
Exclusion Criteria:
- Part 1D: participants who have had a gastrectomy or have dietary or other restrictions
that preclude a 10 hour overnight fast or consumption of the high fat, high calorie
meal
- Part 2B: prior neoadjuvant or adjuvant treatment with a non-steroidal aromatase
inhibitor with disease recurrence while on or within 12 months of completing
treatment. Prior treatment with any CDK4/6 inhibitor
- Part 2C: prior treatment with any CDK inhibitor, fulvestrant, everolimus, or any agent
whose mechanism of action is to inhibit the PI3K-mTOR pathway
- Known active uncontrolled or symptomatic Central Nervous System (CNS) metastases
carcinomatous meningitis, or leptomeningeal disease
- Other active malignancy within 3 years prior to randomization, except for adequately
treated basal cell or squamous cell skin cancer, or carcinoma in situ
- Major surgery or radiation within 4 weeks prior to study intervention
- Last anti-cancer treatment within 2 weeks prior to study intervention
- Participation in other studies involving investigational drug(s) within 4 weeks prior
to study entry
- Pregnant or breastfeeding female participant
- Active inflammatory gastrointestinal (GI) disease, known diverticular disease or
previous gastric resection or lap band surgery including impairment of
gastrointestinal function or GI disease