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

Recruiting now · Phase 1

Conditions studied: Neoplasms, Tenosynovial Giant Cell Tumor

In brief

This is an open-label phase 1 study to determine the safety and tolebility of oral ABSK021 in patients with advanced solid tumor as well as the Recommended Phase 2 dose (RP2D) of oral ABSK021. Preliminary antitumor activity will also be assessed.

Key facts

Study ID

NCT04192344

Run by

Abbisko Therapeutics Co, Ltd

People needed

276

Starts

2020-01-20

Expected to finish

2026-12-31

Last updated by the study team

2026-03-19

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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) :
• 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);
• Measurable disease as defined by RECIST 1.1 (except that a minimal size of 2 cm is required), assessed from MRI scans;
• Others

You may not qualify if…

• 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) :
• Known allergy or hypersensitivity to any component of the investigational drug product
• For expansion part, previous treatment with CSF 1/CSF 1R pathway inhibitors (not applicable for TGCT patients in US）
• Others

Where it is running

• Beijing Jishuitan Hospital — Beijing, Beijing Municipality, China (enrolling)
• The First Affiliated Hospital of Sun Yat-sen University — Guangdong, Guangzhou, China (enrolling)
• Xi'an Hong Hui Hospital — Xian, Shanxi, China (enrolling)
• West China Hospital of Sichuan University — Chengdu, Sichuan, China (enrolling)
• The Second Affiliated Hospital Zhejiang University School of Medicine — Hangzhou, Zhejiang, China (enrolling)
• Henan Cancer Hospital — Zhengzhou, Henan, China
• Precision NextGen Oncology — Beverly Hills, California, United States
• Jiangsu Province Hospital — Nanjing, Jiangsu, China
• Nanjing Drum Tower Hospital — Nanjing, Jiangsu, China
• Liaoning Cancer Hospital — Shenyang, Liaoning, China
• Huashan Hospital of Fudan University — Shanghai, Shanghai Municipality, China
• Shanghai Sixth People's Hospital — Shanghai, Shanghai Municipality, China
• The First Affiliated Hospital of Zhengzhou Universtity — Zhengzhou, Henan, China
• SCRI at HealthOne — Denver, Colorado, United States
• The Winship Cancer Institute of Emory University — Atlanta, Georgia, United States
• MD Anderson Cancer Center — Houston, Texas, United States
• Hebei Medical University Third Hospital — Shijiazhuang, Hebei, China

Full record on ClinicalTrials.gov

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