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A Study to Evaluate the Safety and Tolerability of ETC-1922159 as a Single Agent and in Combination With Pembrolizumab in Advanced Solid Tumours

E

Experimental Drug Development Centre (EDDC)

Status and phase

Active, not recruiting
Phase 1

Conditions

Solid Tumors

Treatments

Drug: Pembrolizumab
Drug: ETC-1922159

Study type

Interventional

Funder types

Other
Industry

Identifiers

Details and patient eligibility

About

This is a Phase 1A/B study consisting of four parts.

  1. Part A (completed) is a non-randomised, open-label, sequential evaluation of the safety, pharmacokinetics (PK), maximum tolerated dose (MTD), and recommended dose (RD) of ETC-1922159 in patients with advanced or metastatic, or unresectable solid malignancies, for whom no approved treatment option or standard of care is available. Dose escalation, with the goal of identifying the MTD and RD, is guided by an ordinal continual reassessment method (oCRM) model with a cohort size of one patient.
  2. Part A extension (completed) is a non-randomised, non-comparative, open-label evaluation of the safety and tolerability of ETC-1922159 together with the bone protective treatment (denosumab) in patients with advanced or metastatic, or unresectable solid malignancies, for whom no approved treatment option or standard of care is available.
  3. Part B dose escalation (completed) is a non-randomised, open-label, sequential evaluation of the MTD, RD, safety, PK, and PD (pharmacodynamics) of ETC 1922159 in combination with pembrolizumab in patients with advanced or metastatic, or unresectable solid malignancies, for whom no approved treatment option or standard of care is available.
  4. Part B dose expansion will be a non-randomised, non-comparative, open-label study evaluation of the safety and tolerability of ETC-1922159 as a single agent until disease progression and then in combination with pembrolizumab at the RD identified in the Part B dose escalation segment, in patients with advanced or metastatic, or unresectable solid malignancies that are refractory, intolerant or not suitable for available treatment according to the treating physician.

It is anticipated that the study will take approximately 78 months to complete (36 months for Part A and Part A Extension, approximately 6 months for Part B dose escalation and approximately 36 months for Part B dose expansion).

Enrollment

89 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria (Part B):

  • 18+ yrs (US), 21+ yrs (Singapore)

  • Ability to give informed consent

  • Histologically/cytologically confirmed advanced or metastatic tumors, that are unresectable solid malignancies, and that are are refractory, intolerant or not suitable to available treatment

  • Objective and radiologically confirmed disease progression at screening

  • Measurable disease by RECIST v1.1

  • ECOG (Eastern Cooperative Oncology Group) 0-2

  • Life expectancy ≥3 months

  • Organ function:

    • Absolute neutrophil count ≥1.0×10^9/L
    • Platelets ≥100×10^9/L (w/o transfusions w/in 21 days)
    • Hemoglobin ≥9 g/dL
    • PT (prothrombin time) and PTT (partial thromboplastin time) w/in ≤1.5× ULN
    • International normalised ration (INR) ≤1.5× ULN Note: If the patient is on allowed anti-coagulants the INR should be in the therapeutic range
    • Total bilirubin ≤1.5× ULN
    • Transaminases (AST and/or alanine aminotransferase) ≤2.5× ULN (<5× ULN with liver metastases)
    • Creatinine clearance ≥60 mL/min
    • Total calcium (corrected for serum albumin) within normal limits

Note: Patients with grade 1 changes can be included as long as they are asymptomatic and can receive supplementation during the study.

  • Magnesium ≥ lower limit of normal (LLN). Note: Patients with grade 1 changes can be included as long as they are asymptomatic and can receive supplementation during the study.

  • Normal urinalysis

    • Patients must have a T-score greater than -1 to be eligible, however, patients with osteopenia (T-score of -1 to -2.5 at L/R total hip, L/R femoral neck or lumbar spine [L1-L4]) are eligible to participate and will receive calcium and vitamin D supplements during the study. Patients with osteoporosis (T-score of < -2.5) must be excluded.
    • Capable of swallowing study medication or has caregiver responsible for administering study drug
    • Negative serum pregnancy test
    • Dose Expansion - Group 1 and Group 2a only (patients with MSS or pMMR [microsatellite stable]-colorectal cancer [CRC]): Is refractory, intolerant or not suitable for treatment with fluoropyrimidine, oxaliplatin, or irinotecan.

Note: patients with advanced or metastatic appendiceal cancer refractory, intolerant to current standard of care, will be considered under the CRC cohort.

  • Dose Expansion - Group 1 patients: MSS or pMMR-CRC with confirmed presence of at least one of the four different recurrent gene fusions involving RSPO2 or RSPO3 (Fusions A-D). Note: If adequate tissue samples are available as determined by the lab or pathologist, patients do not have to wait for the result before enrolment into Group 1 and Group 2a. Patients with indeterminate and/or unreported results may be enrolled into Group 2a, but can be retrospectively assigned to Group 1 once the patient has a confirmed RSPO gene fusion determined as described above.
  • Dose Expansion - Group 2a patients: Has MSS or pMMR-CRC with confirmed absence of all four different recurrent gene fusions involving RSPO2 or RSPO3 (Fusions A-D).
  • Dose Expansion - Groups 2b and 2c only (patients with MSS or pMMR-ovarian and MSS-endometrial cancer): Has advanced or metastatic disease for which further conventional therapy, e.g. platinum-based chemotherapy, is not suitable. Has MSS/pMMR tumours as determined by IHC (immunohistochemistry), PCR (polymerase chain reaction) or NGS (next generation sequencing).
  • Dose expansion segment - Groups 2d only (MSS or pMMR cancers): Has advanced or metastatic disease for which further conventional therapy is not suitable according to the treating physician. Patients with MSS or pMMR solid tumours with molecular phenotypes potentially sensitive to upstream Wnt pathway inhibitors will be recruited.
  • Dose Expansion: Pre-dose and post-dose tumour biopsies are mandatory unless tumour is inaccessible or deemed unsafe for procedure by principal investigator.
  • Archival tumour tissue available (≥40 µm thickness with ≥20% tumour content; plus one 5-µm section for H&E stain:) for all patients that cannot provide a fresh tumour biopsy.

Exclusion Criteria (Part B):

  • Male patient with sexual partner(s) of childbearing potential unwilling to use contraception. Sexually active male patients must use a condom during intercourse during the study and for 12 weeks after the end of treatment. Condom must also be used by vasectomised males.

  • Female of childbearing potential, unless birth control is used during study and for 12 weeks after end of treatment.

  • Pregnant or nursing (lactating) female.

  • Dose Escalation: Current or anti-cancer therapy within 4 weeks pre-study or with Grade ≤1 side effects not resolved within 4 weeks pre-study.

  • Dose Expansion segment: Has received previous treatment with pembrolizumab or immunotherapy treatment within 4 weeks (28 days) prior to starting the study drug is permitted

    • Dose Expansion (Groups 1, 2a, 2b and 2d): Immunotherapy within 4 weeks (28 days) prior to starting study.
    • Dose Expansion (Group 2c MSS endometrial cancer only): Immunotherapy either alone or in combination with lenvatinib within 4 weeks (28 days) prior starting study drug.
  • Is receiving any concomitant anti-cancer therapy.

  • Has used other investigational products within 4 weeks or 5 half-lives (whichever is longer) prior to first dose of study drug.

  • Has evidence of other malignancy not in remission or history of other malignancy within last 3 yrs (exceptions: treated basal or skin squamous cell carcinoma or in situ cancer of cervix)

  • Has central nervous system metastases, unless treated with surgery, whole brain radiation or stereotactic radiosurgery, and stable disease ≥8 weeks without steroid use for ≥4 weeks prior to first dose of study drug.

  • Has received prior radiation therapy within 4 weeks, or limited field radiation within 2 weeks, prior to study drug, or with unresolved Grade ≤1 side effects.

  • Has history of radiation to spine/pelvis bone or chemoradiation to pelvic organs in the last 6 months prior to starting study drug, or the side effects of such therapy have not resolved to Grade ≤1 (NOTE: Such patients can be enrolled as long as they do not have osteoporosis (for details of calculating T-score for eligibility see Inclusion Criterion 9). Patients should initiate concurrent bone protective treatment prophylaxis if any radiation therapy has been given in the last 2 years or they are at high risk of bone related AEs.

  • Has had major surgical procedure within 4 weeks of starting study drug. Or patient has not fully recovered from all surgery-related complications to Grade ≤1.

  • Has a history of interstitial lung disease, sarcoidosis, silicosis, idiopathic pulmonary fibrosis, or pulmonary hypersensitivity pneumonitis.

  • Has received bisphosphonate therapy for osteoporosis or symptomatic hypercalcaemia, or denosumab for osteoporosis prior to starting study drug.

  • Has osteoporosis (T-score of < -2.5 at left or right total hip, left or right femoral neck, or lumbar spine [L1-L4] as determined by DEXA scan at Screening).

  • Has a history of symptomatic vertebral fragility fractures or fragility fracture of hip, pelvis, wrist, or other location (fragility fracture - any fracture without trauma or as a result of a fall from ≤standing height).

  • Has moderate (25%-40% decrease vertebral height) or severe (>40% decrease vertebral height) morphometric vertebral fractures.

  • Has ß-CTX serum level >600 pg/mL in the morning after at least 10 hours of fasting at Screening. Note: If patients meet the exclusion criteria of ß-CTX serum level >600 pg/mL in the morning after at least 10 hours of fasting at screening, patient can begin their treatment with the bone protective treatment (denosumab with a starting dose of 120 mg, administered SC) as long as the patient has a ß-CTX serum level ≤1000 pg/mL.

  • Has thyrotropin level less than lower limit of normal (LLN).

  • Has 25-hydroxy vitamin D levels less than 25 mmol/L (10 ng/mL).

  • Has bone metastases.

  • Has a history of long QT or prolonged QTc (>460 ms).

  • Is receiving, or has received thiazolidinedione peroxisome proliferator-activated receptor gamma agonist (e.g. Actos® [pioglitazone] and Avandia® [rosiglitazone]) w/in 4 wks prior to starting study drug.

  • Has metabolic bone disease such as hyperparathyroidism, Paget's disease or osteomalacia.

  • Has a known clinically significant bleeding disorder or coagulopathy.

  • Is receiving or has received within 4 weeks prior to starting study drug, heparin, warfarin or similar anti-coagulants except for patients on low molecular weight heparin or Direct-Acting Oral Anticoagulants (DOACs: factor Xa or direct thrombin inhibitors) for treatment or prophylaxis.

  • Has severe or unstable medical conditions such as heart failure, ischemic heart disease, uncontrolled hypertension, uncontrolled diabetes mellitus, psychiatric condition, ongoing cardiac arrhythmia requiring medication (Grade ≥2, by National Cancer Institute [NCI] CTCAE v. 4.03).

  • Has a known history of human immunodeficiency virus (HIV) or active bacterial, viral or fungal infections.

  • Has a history of gastric bypass surgery.

  • Has received prior treatment with an inhibitor of the Wnt-B-catenin pathway.

  • Is unwilling or unable to comply with the protocol.

  • Cannot start treatment with the bone protective treatment with denosumab and/or zoledronic acid. Cannot start treatment with the bone protective treatment with denosumab SC, in patients requiring this treatment at the start of the study.

  • Dose Expansion: Patient is unable to provide tumour tissue (from archival tissue or a fresh biopsy or tumour RNA).

  • Has received prophylactic administration of hematopoietic colony stimulating factors within 4 weeks prior to starting study drug.

  • Is receiving active treatment with an oral or IV glucocorticoid for ≥4 weeks at a daily dose equivalent to ≥10 mg of oral prednisone within the 12 weeks prior to starting the study drug.

  • Has recent or current active infectious disease requiring systemic antibiotics or antifungal or antiviral treatment within 2 weeks prior to the start of the study drug. Subjects receiving prophylactic antibiotics (e.g. for prevention of urinary tract infection or chronic obstructive pulmonary disease) are eligible.

  • Has a serious non-healing wound.

  • Has a history of vasculitis.

  • Has an active autoimmune disease that has required systemic treatment in the past 2 years. Replacement therapy is not considered a form of systemic treatment.

  • Has received a live vaccine within 28 days prior to the start of study drug or anticipate that such live vaccine will be required during the study. Anti-SARS-CoV-2 live virus vaccines developed that utilised a replication-deficient simian adenoviral vector (ChAdOx1) should be avoided.

Other protocol-defined inclusion and exclusion criteria may apply.

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Sequential Assignment

Masking

None (Open label)

89 participants in 2 patient groups

Dose Escalation
Experimental group
Description:
ETC-1922159 + pembrolizumab
Treatment:
Drug: ETC-1922159
Drug: Pembrolizumab
Dose Expansion
Experimental group
Description:
ETC-1922159 as single agent until disease progression, then in combination with pembrolizumab at the recommended dose (RD) identified in the dose escalation segment
Treatment:
Drug: ETC-1922159
Drug: Pembrolizumab

Trial contacts and locations

11

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Central trial contact

Veronica Diermayr; Venkateshan Srirangam Prativadibhayankara, MD

Data sourced from clinicaltrials.gov

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