A Study to Assess the Safety, Tolerability, and Pharmacokinetics of ABSK-021 in Patients With Advanced Solid Tumor

Launched by ABBISKO THERAPEUTICS CO, LTD · Dec 9, 2019

Keywords

ClinConnect Summary

This clinical trial is evaluating a new medication called ABSK-021 for patients with advanced solid tumors, including a specific type of tumor known as tenosynovial giant cell tumor (TGCT). The main goals of the study are to see how safe the medication is, how well it is tolerated by patients, and to determine the best dose for future studies. Researchers will also look for any signs that the drug might help shrink tumors.

To be eligible for this trial, participants should have a confirmed diagnosis of a solid tumor that has either worsened after standard treatments or for which no standard treatment exists. Patients should be aged 18 or older and have a life expectancy of at least three months. Those interested in joining the trial will take ABSK-021 as a pill. Throughout the study, participants will be monitored closely for any side effects and how their tumors respond to the treatment. It’s important to know that certain health conditions and previous treatments may prevent someone from participating, so discussing eligibility with a doctor is essential.

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Eligibility criteria

• Inclusion Criteria:
• • Histologically confirmed solid tumors that have progressed on or intolerant to standard therapy or whom no standard therapy exists
• • ECOG (electrocorticogram) performance status 0\~1
• • Life expectancy ≥ 3 months
• • Adequate organ function and bone marrow function
• For patients with tenosynovial giant cell tumor (TGCT) :
• • 1. A diagnosis of TGCT \[i ncluding pigmented villonodular synovitis (PVNS) or giant cell tumors of the tendon sheath (GCT TS) (i) that has been histologically confirmed either by a pathologist at the treating institution or a central pathologist, and (ii) where surgical resection would be associated with potentially worsening functional limitation or severe morbidity (locally advanced disease), with morbidity determined consensually by qualified personnel (eg, two surgeons or a multi disciplinary tumor board);
• • 2. Measurable disease as defined by RECIST 1.1 (except that a minimal size of 2 cm is required), assessed from MRI scans;
• • 3. Others
• Exclusion Criteria:
• • Known allergy or hypersensitivity to any component of the investigational drug product Previous treatment with CSF-1(colony stimulating factor 1)/CSF-1R (colony stimulating factor 1 receptor) pathway inhibitors
• • Known additional malignancy that is progressing or required active treatment within 3 years of the first dose of study treatment
• • Inability to take oral medication or significant nausea and vomiting, malabsorption, external biliary shunt, or significant bowel resection that would preclude adequate absorption of oral medication
• • Previous anti-cancer therapy, including chemotherapy, radiotherapy, endocrine therapy or molecular targeted therapy within ≤ 5-halflife or ≤ 4 weeks (whichever is shorter) prior to initiation of study treatment (chemotherapy with nitrosourea or mitomycin should be 6 weeks prior to initiation of study treatment)
• • Major surgery within 4 weeks of the first dose of study drug and all surgical wounds must be healed and free of infection or dehiscence
• • Prior toxicities from chemotherapy, radiotherapy, and other anti-cancer therapies, including immunotherapy that have not regressed to Grade ≤2 severity (CTCAE v5.0) with the exception of alopecia and vitiligo
• • Prior corticosteroids as anti-cancer therapy within a minimum of 2 weeks of the first dose of study drug
• • Concomitant use of strong inhibitors or inducers of CYP3A4
• • Active central nervous system (CNS) metastases
• • Impaired cardiac function or clinically significant cardiac disease
• • Patients with Gilbert's Syndrome or other underlying conditions that may lead to a greater likelihood of developing LFT(liver function test) abnormalities during the study
• • Known human immunodeficiency virus or active hepatitis B, or active hepatitis C infection
• • Refractory/uncontrolled ascites or pleural effusion
• • Pregnant or nursing
• For patients with tenosynovial giant cell tumor (TGCT) :
• • 1. Known allergy or hypersensitivity to any component of the investigational drug product
• • 2. For expansion part, previous treatment with CSF 1/CSF 1R pathway inhibitors (not applicable for TGCT patients in US）
• • 3. Others