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First-in-Human Study of Mutant-selective PI3Kα Inhibitor, RLY-2608, as a Single Agent in Patients With Advanced Solid Tumors and in Combination With Endocrine Therapy +/- a CDK4/6 or CDK4 Inhibitor in Patients With Advanced Solid Tumors or Advanced Breast Cancer
NCT05216432 · Relay Therapeutics, Inc.
In plain English
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About this study
This is an open-label, FIH study designed to evaluate the maximum tolerated dose, recommended Phase 2 dose, safety, tolerability, PK, pharmacodynamics, and preliminary antineoplastic activity of RLY-2608, in advanced solid tumor patients with a Phosphatidylinositol-4,5-bisphosphate-3 kinase, catalytic subunit alpha (PIK3CA) mutation in blood and/or tumor per local assessment. The study will evaluate RLY-2608 as a single agent for patients with unresectable or metastatic solid tumors. It will also evaluate RLY-2608 in combination RLY-2608 + fulvestrant and in triple combination RLY-2608 + fulvestrant + CDK4/6 inhibitor (palbociclib or ribociclib) or CDK4 inhibitor (PF-07220060) for patients with HR+ HER2- locally advanced or metastatic breast cancer. The RLY-2608 single agent arm, RLY-2608 + fulvestrant combination arm, and triple combination arms will have 2 parts: a dose escalation (Part 1) and a dose expansion (Part 2).
Eligibility criteria
Key Inclusion Criteria
Patient has ECOG performance status of 0-1
One or more documented primary oncogenic PIK3CA mutation(s) in blood and/or tumor per local assessment
Other potentially oncogenic PIK3CA mutations may be considered but must be approved by the Sponsor prior to enrollment.
Part 1 \[Escalation\] - Ability to provide archived tumor tissue or be willing to undergo pretreatment tumor biopsy to assess PIK3CA status retrospectively Part 2 \[Expansion\] - Submit tumor tissue prior to study drug initiation for determination of PIK3CA mutation retrospectively.
Key Inclusion for RLY-2608 Single Agent Arm
* \[For Part 1: Escalation\]: Evaluable disease per RECIST v1.1
* \[For Part 2: Expansion\]: Measurable disease per RECIST v1.1
* Disease that is refractory to standard therapy, intolerant to standard therapy, or has declined standard therapy.
* Part 1- histologically or cytologically confirmed diagnosis of unresectable or metastatic solid tumor
* Part 2 - Unresectable or metastatic solid tumor with PIK3CA mutation(s) and one of the following tumor types:
Group 1: clear cell ovarian cancer Group 2: head and neck squamous cell carcinoma Group 3: cervical cancer Group 4: other solid tumors, excluding colorectal, clear cell ovarian, head and neck squamous cell, and cervical cancers Group 5: unresectable or metastatic solid tumors with PIK3CA double mutations In addition, the SRC (with Sponsor approval) may choose to open additional group(s) of 20 participants to study the clinical activity, safety, and PK/PD with other specified solid tumor types.
Key Inclusion for Combination Arms:
* Doublet combination arms \[Part 1 and Part 2\]: Evaluable disease per RECIST v1.1
* Triplet combination arms:
* \[Part 1 and Part 2 Dose Expansion, Group 1\]: Evaluable disease per RECIST.
* \[Part 2 Dose Expansion, Group 2\]: Measurable disease per RECIST. Bone-only lytic or lytic/blastic disease with at least 1 measurable soft-tissue component per RECIST may be eligible.
* \[For Part 1 and Part 2\]: Male or female with histologically or cytologically confirmed diagnosis of HR+, HER2- unresectable or metastatic breast cancer that is not amenable to curative therapy. Females may be postmenopausal, premenopausal, or perimenopausal. Premenopausal or perimenopausal females must have a histologically or cytologically confirmed diagnosis of HR+ HER2- locally advanced or metastatic breast cancer that is not amenable to curative therapy and must have initiated treatment with a gonadotropin-releasing hormone (GnRH) agonist at least 4 weeks prior to start of study drug with continuation of GnRH agonist for the duration of study treatment (GnRH agonist recommended for males).
* Had previous treatment for breast cancer with: \[Does not apply to triplet combination arms, Part 2 Dose Expansion, Group 2\]:
1. ≤1 line of chemotherapy in the metastatic setting
2. ≥1 CDK4/6 inhibitor in either the adjuvant and/or metastatic setting
3. ≥1 antiestrogen therapy in either adjuvant and/or metastatic setting, including, but not limited to, selective estrogen-receptor degraders (eg, fulvestrant), selective estrogen receptor modulators (eg, tamoxifen), and aromatase inhibitors (AI) (letrozole, anastrozole, exemestane), and
4. ≥1 PARP inhibitor, if appropriate, if documented germline BRCA1/2 mutation Note: Systemic local, loco-regional, or adjuvant treatment with chemotherapy and PARP inhibitors is not to be included in enumeration or previous treatment
\[For double combination arm; Part 2 Dose Expansion, Group 2\]: Received prior treatment with a PI3Kα, AKT, or mTOR inhibitor and discontinued the inhibitor due to intolerance and not disease progression, where intolerance is defined as treatment discontinuation due to treatment related AE (eg. hyperglycemia, rash, diarrhea, stomatitis) other than severe hypersensitivity reaction and/or life-threatening reactions, such as anaphylaxis and Stevens-Johnson syndrome.
\[For triple combination arms; Part 1 dose escalation\]: Participants who had previous treatment for breast cancer with PI3Kα, AKT, mTOR inhibitors and discontiuned due to participant/physician decision, intolerance, or disease progression will be considered.
\[For triple combination arms, Part 2 Dose Expansion, Group 2\]: Participants must be intolerant to or have declined standard therapy for locally advanced or metastatic HR+/HER2- PIK3CA-mutated breast cancer. Prior endocrine therapy and CDK4/6inhibitors are allowed as follows:
1. Participants must have progressed during (neo)adjuvant endocrine therapy or within12 months of completing (neo)adjuvant endocrine therapy with an AI or tamoxifen.
2. If a CDK4/6 inhibitor was included as part of (neo)adjuvant therapy, disease must have recurred/progressed \>12 months after completion of the CDK4/6 inhibitor portion of (neo)adjuvant therapy
Key Exclusion Criteria
Prior treatment with:
1. PI3Kα, AKT, or mTOR inhibitors (all arms except for doublet RLY-2608 + fulvestrant arm, Part 2, Group 2; and triplet combinations, Part 1 dose escalation).
2. Immune checkpoint inhibitors.
3. Triplet combinations RLY-2608 + CDK4 or CDK4/6 inhibitor + fulvestrant, Part 2 expansion, Group 2 only:
i. Prior systemic chemotherapy or antibody drug conjugate for locally advanced or metastatic disease. ii. Prior CDK2, CDK4, or CDK4/6 inhibitor as treatment for locally advanced or metastatic disease.
iii. Prior treatment with fulvestrant or any selective ER degrader, with the exception of patients who have received fulvestrant or any selective ER degrader as part of neoadjuvant therapy only and with treatment duration ≤6 months.
Type 1 or Type 2 diabetes requiring antihyperglycemic medication, or fasting plasma glucose ≥140 mg/dL and glycosylated hemoglobin (HbA1c) ≥7.0%.
History of allergy or hypersensitivity to any components or excipients of PI3K inhibitors. For combination arms only: allergy or hypersensitivity to any components or excipients of fulvestrant, palbociclib, ribociclib, and/or PF-07220060 as appropriate for the combination.
Past medical history of or ongoing ILD, or pneumonitis requiring intervention. Participants with past history of resolved Grade 1 pneumonitis may be considered, except in triple combination arms.
The following cardiac criteria:
* Mean resting corrected QT interval (QTc) \>460 msec
* For triple combination arm with ribociclib: Mean QTcF ≥450 msec (this is what we confirmed is shown in the redacted version of the protocol.
CNS metastases or primary CNS tumor that is associated with progressive neurologic symptoms
Study design
Enrollment target: 930 participants
Allocation: non_randomized
Masking: none
Age groups: adult, older_adult
Timeline
Starts: 2021-12-08
Estimated completion: 2027-04-30
Last updated: 2025-09-22
Interventions
Drug: RLY-2608Drug: FulvestrantDrug: Palbociclib 125mgDrug: Ribociclib 400mgDrug: Ribociclib 600mgDrug: PF-07220060 100mgDrug: PF-07220060 300 mg
Primary outcomes
- • Determination of maximum tolerated dose (MTD) and/or recommended Phase 2 dose (RP2D) of RLY-2608 as a single agent (Cycle 1 (4-week cycle) of treatment for MTD and at the end of every cycle (4-week cycles) for RP2D until study discontinuation, approximately 24 months)
- • Determination of maximum tolerated dose (MTD) and/or recommended Phase 2 dose (RP2D) of RLY-2608 in combination with fulvestrant (Cycle 1 (4-week cycle) of treatment for MTD and at the end of every cycle (4-week cycles) for RP2D until study discontinuation, approximately 24 months)
- • Determination of maximum tolerated dose (MTD) and/or recommended Phase 2 dose (RP2D) of RLY-2608 in combination with fulvestrant and a CDK 4/6 inhibitor (palbociclib, ribociclib), and in combination with CDK4 inhibitor (PF-07220060) and fulvestrant (Cycle 1 (4-week cycle) of treatment for MTD and at the end of every cycle (4-week cycles) for RP2D until study discontinuation, approximately 24 months)
Sponsor
Relay Therapeutics, Inc. · industry
Contacts & investigators
ContactRelay Therapeutics Inc · contact · ClinicalTrials@relaytx.com · 617-322-0731
All locations (37)
The University of Arizona Cancer CenterRecruiting
Tucson, Arizona, United States
University of California-San DiegoRecruiting
San Diego, California, United States
HealthONERecruiting
Denver, Colorado, United States
Yale UniversityRecruiting
New Haven, Connecticut, United States
Florida Cancer SpecialistsRecruiting
Orlando, Florida, United States
Boca Raton Clinical Research (BRCR) GlobalWithdrawn
Plantation, Florida, United States
University of Chicago Medical CenterRecruiting
Chicago, Illinois, United States
Community Health NetworkRecruiting
Indianapolis, Indiana, United States
Massachusetts General HospitalRecruiting
Boston, Massachusetts, United States
Dana-Farber Cancer InstituteRecruiting
Boston, Massachusetts, United States
University of MichiganRecruiting
Ann Arbor, Michigan, United States
Washington University School of Medicine St. LouisRecruiting
St Louis, Missouri, United States
Renown Regional Medical CenterRecruiting
Reno, Nevada, United States
Rutgers UniversityRecruiting
New Brunswick, New Jersey, United States
NYU LangoneRecruiting
New York, New York, United States
Columbia University Herbert Irving Comprehensive Cancer CenterRecruiting
New York, New York, United States
Memorial Sloan KetteringRecruiting
New York, New York, United States
Tennessee OncologyRecruiting
Nashville, Tennessee, United States
University of Texas Southwestern Medical CenterRecruiting
Dallas, Texas, United States
The University of Texas M.D. Anderson Cancer CenterRecruiting
Houston, Texas, United States
University of Utah- Huntsman Cancer CenterRecruiting
Salt Lake City, Utah, United States
Inova Schar Cancer CenterRecruiting
Fairfax, Virginia, United States
NEXT VirginiaRecruiting
Fairfax, Virginia, United States
UW Carbone Cancer CenterRecruiting
Madison, Wisconsin, United States
St Vincents HospitalRecruiting
Sydney, New South Wales, Australia
Peter MacCallum Cancer CenterRecruiting
Melbourne, Victoria, Australia
The Alfred HospitalRecruiting
Melbourne, Victoria, Australia
Centre Léon BérardRecruiting
Lyon, Auvergne-Rhône-Alpes, France
Institute BergoniéRecruiting
Bordeaux, France
Gustave RoussyRecruiting
Villejuif, France
Istituto Europeo di Oncologia IRCCSRecruiting
Milan, Italy
Vall d'Hebron Instituto de OncologiaRecruiting
Barcelona, Barcelona, Spain
START BarcelonaRecruiting
Barcelona, Catalonia, Spain
Instituto Valenciano de OncologiaRecruiting
Valencia, Valencia, Spain
Institut Catala D'Oncologia - Badalona (ICO Badalona)Recruiting
Barcelona, Spain
START Madrid - Hospital Fundacion Jimenez DiazRecruiting
Madrid, Spain
Hospital Universitario 12 de OctubreRecruiting
Madrid, Spain