Sponsor: M.D. Anderson Cancer Center (other)
Phase: 2
Start date: Dec. 5, 2025
Planned enrollment: 70
Zanzalintinib (XL092) is an investigational, orally administered multikinase inhibitor being developed for solid tumors, both alone and with immune-checkpoint inhibitors. The most mature evidence comes from metastatic colorectal cancer (mCRC); studies are also evaluating renal cell, head and neck, prostate, liver, and other cancers. (pubmed.ncbi.nlm.nih.gov)
Zanzalintinib inhibits receptor tyrosine kinases involved in angiogenesis, tumor growth, metastasis, treatment resistance, and immune suppression—notably VEGFR2, MET, and the TAM-family kinases TYRO3, AXL, and MER. This profile provides the rationale for combining it with PD-1/PD-L1 checkpoint inhibitors. Its reported half-life of approximately 16–22 hours supports once-daily dosing. (cancer.gov)
Metastatic colorectal cancer: In the randomized phase 3 STELLAR-303 trial, 901 previously treated patients with non-MSI-H/non-dMMR mCRC received zanzalintinib plus atezolizumab or regorafenib. Median overall survival was 10.9 versus 9.4 months, respectively (hazard ratio 0.80; 95% CI 0.69–0.93; p=0.0045). Objective response rates were 4% versus 1%, and disease-control rates were 54% versus 41%. In the subgroup without liver metastases, final median survival was 15.9 versus 12.7 months, but the difference was not statistically significant (HR 0.83; p=0.1185). (pubmed.ncbi.nlm.nih.gov)
Earlier phase 1 STELLAR-001 results in refractory mCRC found response rates of 7.4% with zanzalintinib–atezolizumab and 1.9% with zanzalintinib alone; median progression-free survival was 4.0 and 3.0 months, respectively. (ascopubs.org)
Renal cell carcinoma: Early, nonrandomized results also suggest activity. Single-agent zanzalintinib produced a 38% response rate and 88% disease-control rate in 32 previously treated patients with clear-cell RCC. In first-line STELLAR-002, zanzalintinib plus nivolumab produced a 63% response rate in 40 patients, whereas the combination with nivolumab and relatlimab produced a 33% response rate in a separate 40-patient cohort. These findings remain preliminary and require confirmation in randomized trials. (ascopubs.org)
In STELLAR-303, grade 3 or worse treatment-related adverse events occurred in 60% of patients receiving zanzalintinib–atezolizumab and 37% receiving regorafenib. The most common severe treatment-related events with the combination were hypertension (15%), proteinuria (6%), fatigue (6%), and diarrhea (6%). Treatment-related deaths occurred in five patients (1%) receiving the combination and one patient receiving regorafenib. (pubmed.ncbi.nlm.nih.gov)
Across early studies, frequently reported toxicities included diarrhea, nausea, decreased appetite, fatigue, and hypertension. Dose reductions were common in the renal-cell carcinoma combinations, although treatment discontinuation rates were relatively low in the zanzalintinib–nivolumab cohort. (ascopubs.org)
Last updated: Sep 2026
Goal: Evaluate the activity and safety of zanzalintinib monotherapy in advanced or metastatic bone sarcomas.
Patients: Adults with measurable, unresectable locally advanced or metastatic osteosarcoma, Ewing sarcoma, grade 2–3 conventional chondrosarcoma, or another primary bone sarcoma. Patients generally must have received at least one prior systemic therapy, unless no standard treatment exists, and no more than two lines for advanced disease. ECOG performance status must be 0–2. Prior VEGF-targeted tyrosine kinase inhibitors are excluded.
Design: Nonrandomized, four-cohort study organized by sarcoma subtype. All participants receive the investigational treatment; there is no control arm.
Treatments: Participants receive zanzalintinib alone. Zanzalintinib is an oral multikinase inhibitor targeting VEGFR2, MET, and the TAM-family kinases TYRO3, AXL, and MER, which are involved in angiogenesis and tumor progression. Early single-agent studies have shown activity in other cancers, including a 38% response rate in a small previously treated clear-cell renal cell carcinoma cohort; efficacy in bone sarcoma remains to be established.
Outcomes: The stated efficacy objectives are progression-free survival at 16 weeks for osteosarcoma and at 12 weeks for the other cohorts. Secondary measures include RECIST 1.1 objective response rate, progression-free survival, overall survival, and CTCAE v5.0 toxicity. The listed primary outcome also specifies adverse-event incidence through study completion. Exploratory analyses will correlate biomarkers in pretreatment and on-treatment tumor biopsies with clinical benefit.
Burden on patient: Moderate. Oral treatment avoids infusion visits, but participants will need follow-up for imaging and toxicity assessment and must co-enroll in a specimen-collection protocol. Planned pretreatment and on-treatment tumor biopsies add procedures and visits beyond routine care. Visit and scan frequency are not specified.
Last updated: Sep 2026
Inclusion Criteria:
• Patients ≥ 18 years old with pathologically confirmed unresectable locally advanced or metastatic bone sarcoma in one of the following categories: Cohort A - Osteosarcoma, Cohort B - Ewing sarcoma, Cohort C - Chondrosarcoma (conventional, grades 2-3), Cohort D - Other primary sarcoma of bone including but not limited to dedifferentiated chondrosarcoma, undifferentiated pleomorphic sarcoma (UPS) of bone, chordoma, and non-Ewing's round cell sarcomas of bone.
chondrosarcoma, undifferentiated pleomorphic sarcoma (UPS) of bone, chordoma, and non-Ewing's round cell sarcomas of bone.
* Patients with conventional chondrosarcoma (Cohort C) must demonstrate evidence of disease progression by RECIST 1.1 within 12 weeks of trial enrollment
* Patients must have relapsed or become refractory to conventional therapy, receiving at least 1 prior line of systemic therapy unless no standard of care exists.
* Patients may have received no more than 2 prior lines of systemic therapy in the advanced/metastatic setting.
* Multi-agent and/or alternating neoadjuvant/adjuvant standard of care chemotherapy will be counted as 1 line of systemic therapy if given for metastatic disease. Otherwise, neoadjuvant/adjuvant chemotherapy for localized disease does not apply towards the limitation regarding prior lines of systemic therapy.
* Patients must have a performance status corresponding to ECOG scores of 0, 1 or 2 (Karnofsky ≥60%).
* Weight \>/= 40 kg.
* Patients must have measurable disease per RECIST v1.1
* Prior radiation will be allowed assuming there is measurable disease based upon RECIST 1.1 and at least 21 days from the completion of all radiation prior to initiation of study treatment. (Note: Previously irradiated lesions can be considered as measurable disease only if progressive disease has been unequivocally documented at that site since radiation)
* Hematological function, as follows:
* Absolute neutrophil count (ANC) ≥ 1500/mm3 (growth factor/G-CSF permitted)
* Platelet count ≥ 100,000/mm3
* Hemoglobin \> 9 g/dL.
* INR ≤ 1.5 and activated partial thromboplastin time (aPTT) \< 1.2 x upper limit of normal (ULN), except subjects on anticoagulation.
* Renal function as follows: calculated creatinine clearance ≥ 40 mL/min (≥ 0.67 mL/sec) using the Cockcroft Gault equation.
* Hepatic function as follows: aspartate aminotransferase (AST) and alanine aminotransferase (ALT) \< 3 x ULN and total bilirubin ≤ 1.5 x ULN (for subjects with Gilberts's disease ≤ 3 x ULN), serum albumin ≥ 2.
* All patients must agree to consent and co-enroll on MD Anderson MOSAIC protocol to allow for sample collection and correlative studies
* For patients with evidence of chronic hepatitis B virus (HBV) infection, the HBV viral load must be undetectable on suppressive therapy, if indicated.
* Patients with a history of hepatitis C virus (HCV) infection must have been treated and cured. For patients with HCV infection who are currently on treatment, they are eligible if they have an undetectable HCV viral load.
* Patients with treated brain metastases are eligible if follow-up brain imaging after central nervous system (CNS)-directed therapy shows no evidence of progression.
* Patients with a prior malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial.
* Patients with known history or current symptoms of cardiac disease, or history of treatment with cardiotoxic agents, should have a clinical risk assessment of cardiac function using the New York Heart Association Functional Classification. To be eligible for this trial, patients should be class 2B or better.
* Female subjects of childbearing potential must not be pregnant at screening. Female subjects are considered to be of childbearing potential unless one of the following criteria is met: permanent sterilization (hysterectomy, bilateral salpingectomy, or bilateral oophorectomy) or documented postmenopausal status (defined as 12 months of amenorrhea in a woman \> 45 years-of-age in the absence of other biological or physiological causes. In addition, females \< 55 years-of-age must have a serum follicle stimulating hormone \[FSH\] level \> 40 mIU/mL to confirm menopause). Note: Documentation may include review of medical records, medical examination, or medical history interview by study site staff.
* Sexually active fertile subjects and their partners must agree to use highly effective method of contraception (hormonal or barrier method of birth control, intrauterine device, tubal ligation or hysterectomy, subject/partner post vasectomy, implantable or injectable contraceptives, condoms, or abstinence) prior to study entry and for the duration of study participation. (Refer to Pregnancy Assessment Policy MD Anderson Institutional Policy # CLN1114). This includes all female patients, between the onset of menses (as early as 8 years of age) and 55 years unless the patient presents with an applicable exclusionary factor which may be one of the following:
* Postmenopausal (no menses in greater than or equal to 12 consecutive months).
* History of hysterectomy or bilateral salpingo-oophorectomy.
* Ovarian failure (Follicle Stimulating Hormone and Estradiol in menopausal range, who have received Whole Pelvic Radiation Therapy).
* History of bilateral tubal ligation or another surgical sterilization procedure.
In addition, men must agree not to donate sperm through 96 days after the last dose of zanzalintinib and women (WOCBP) must agree not to donate effs (ova, oocyte) for the purpose of reproduction for at least 186 days after the last dose of zanalintinib.
• Ability to understand and the willingness to sign a written informed consent document.
Exclusion Criteria:
Prior treatment with zanzalintinib.
* Patients with primary soft tissue sarcoma with metastasis to bone.
o Patients with histologically confirmed Ewing's sarcoma with either bone or soft tissue primary site are eligible for enrollment in Cohort B
* Patients with known sensitivity to the study agents and/or previously identified allergy or hypersensitivity to components of treatment
* Patients previously treated with other VEGF-targeted TKIs (including but not limited to cabozantinib, regorafenib, pazopanib, or similar).
* Receipt of any small molecule kinase inhibitor (including investigational within 2 weeks before first dose of study treatment.
* Untreated central nervous system metastatic disease, leptomeningeal disease, or cord compression.
* Active infection requiring intravenous (IV) antibiotics within 2 weeks of study enrollment.
* Prior receipt of an investigational study drug and/or procedure within 21 days of study day 1.
* Anti-tumor therapy within 21 days of study day 1 including chemotherapy, antibody therapy, or other investigational agent.
* Radiation therapy for bone metastasis within 2 weeks, any other radiation therapy within 4 weeks, or systemic treatment with radionuclides within 6 weeks before first dose of study treatment; ongoing clinically relevant complications from prior radiation therapy are not eligible.
* Any complementary medicine such as herbal supplements, Chinese medicines, or other non-prescription medications being used for the treatment of bone sarcoma within 2 weeks prior to first dose of treatment as detailed in section5.5.
* History of cardiac disease: congestive heart failure New York Heart Association (NYHA) class \> II, unstable angina (angina symptoms at rest), new-onset angina (within the past 6 months before study entry), myocardial infarction within the past 6 months before study entry.
* Uncontrolled hypertension defined as sustained blood pressure (BP) \> 140 mm Hg systolic or \> 90 mm Hg diastolic despite optimal antihypertensive treatment
* Moderate or severe hepatic impairment, i.e. Child-Pugh class B or C.
* Patients with known human immunodeficiency virus (HIV) infection with detectable viral load.
HIV-infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months are eligible for this trial.
* Known infection with acute or chronic hepatitis B or C.
* History of solid organ or allogeneic stem cell transplant
* Any other known concurrent or prior malignancy at time of or within 2 years of first does of study treatment. Prior malignancy that is in remission or otherwsie has not required treatment in \> 2 years will be permitted.
* Stroke (including transient ischemic attack \[TIA\]), myocardial infarction (MI), or other ischemic event, or thromboembolic event (e.g., deep venous thrombosis, pulmonary embolism) within 6 months before first dose of study treatment.
* Pulmonary embolism (PE) or deep vein thrombosis (DVT) or prior clinically significant venous events within 3 months before first dose of study treatment. Note, patients with a diagnosis of incidental, subsegmental PE or DVT within 6 months are allowed if stable, asymptomatic, and treated with a stable dose of permitted anticoagulation (see exclusion criterion) for at least 1 week before first dose of study treatment.
* Gastrointestinal (GI) disorders including those associated with a high risk of perforation or fistula formation:
* Tumors invading the GI-tract from external viscera
* Active peptic ulcer disease, inflammatory bowel disease, diverticulitis, cholecystitis, symptomatic cholangitis or appendicitis, or acute pancreatitis
* Acute obstruction of the bowel, gastric outlet, or pancreatic or biliary duct within 6 months before first dose unless cause of obstruction is definitively managed and asymptomatic
* Abdominal fistula, GI perforation, bowel obstruction, or intra-abdominal abscess within 6 months of the first dose. Note, complete healing of an intra-abdomninal abscess must be confirmed before first dose of study treatment
* Known gastric or esophageal varices
* Ascites, pleural effusion, or pericardial effusion requiring drainage in last 4 weeks
* Clinically significant hematuria, hematemesis, or hemoptysis of \> 0.5 teaspoon (2.5 ml) of red blood, or other history of significant bleeding (eg, pulmonary hemorrhage) within 12 weeks before first dose of study treatment.
* Symptomatic cavitating pulmonary lesion(s) or endobronchial disease. Note, asymptomatic or radiated lesions allowed
* Lesions invading major blood vessel including but not limited to inferior vena cava, pulmonary artery, or aorta. Note, patients with intravascular tumor extension (i.e. tumor thrombus in renal vein or inferior vena cava) may be eligible following Principal Investigator approval
* Other clinically significant disorders that would preclude safe study participation:
* Serious non-healing wound, ulcer, or bone fracture. Note, non-healing wounds or ulcers may be permitted if due to tumor associated skin lesions
* Malabsoprtion syndromes
* Pharmacologically uncompensated, symptomatic hypothyroidism
* Requirement for hemodialysis or peritoneal dialysis
* History of solid organ or allogeneic stem cell transplant
* Major surgery (i.e. GI surgery, removal or biopsy of brain metastasis) within 8 weeks prior to first dose of study treatment. Prior laproscopic surgeries withint 4 weeks prior to first dose of study treatment. Minor surgery (i.e. simple excision, tooth extraction) within 5 days before first dose of study treatment. Complete wound healing from major or minor surgery must have occurred at least prior to first dose of study treatment. Note, fresh/pre-treatment tumor biopsies should be completed at least 5 days prior to the first dose of study treatment. Patients with clinically relevant ongoing complications of prior surgical procedures, including biopsies, are not eligible.
* Corrected QT interval calculated by the Fridericia formula (QTcF) \> 470 ms within 14 days per electrocardiogram (ECG) before first dose of study treatment. Note: Triplicate ECG evaluations will be performed and the average of these 3 consecutive results for QTcF will be used to determine eligibility.
* Patients with psychiatric illness/social situations that would limit compliance with study requirements.
* Pregnant or lactating women are excluded from this study because zanzalintinib is an agent with the potential for teratogenic or abortifacient effects. Because there is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the mother with zanzalintinib, breastfeeding should be discontinued if the mother is treated with zanzalintinib. These potential risks may also apply to other agents used in this study.
* Inability to swallow tablets or ingest a suspension either orally or by nasogastric (NG) or gastronomy (PEG) tube.
* Concomitant anticoagulation with oral anticoagulants (eg, warfarin, direct thrombin inhibitors ) and platelet inhibitors (eg, clopidogrel). Allowed anticoagulants are the following:
* Prophylactic use of low-dose aspirin for cardio-protection (per local applicable guidelines) and low-dose low molecular weight heparins (LMWH).
* Therapeutic doses of LMWH or anticoagulation with direct factor Xa inhibitors rivaroxaban, edoxaban, or apixaban in subjects without known brain metastases who are on a stable dose of the anticoagulant for at least 1 week before first dose of study treatment without clinically significant hemorrhagic complications from the anticoagulation regimen.
* Note, Subjects must have discontinued prohibited oral anticoagulants at least 3 days or 5 half-lives prior to the first dose of study treatment, whichever is longer
* Proteinuria \> 1g/day.
* Other conditions, which in the opinion of the investigator, would compromise the safety of the patient's ability to complete the study
Houston, Texas, 77030, United States
[email protected] / 713-792-3626
Status: Recruiting