Advanced Solid TumorPhase 1NCT05768932
BAL0891 in Patients With Advanced Solid Tumors or Relapsed or Refractory Acute Myeloid Leukemia
A Phase 1 study testing BAL0891, Tislelizumab and Paclitaxel in people with Advanced Solid Tumor and TNBC - Triple-Negative Breast Cancer, run by SillaJen, Inc. at 17 sites in 2 countries.
Trial summary
This study is a multiple cohort, multicenter, open-label Phase 1 study with dose-escalation substudies investigating intravenous (IV) BAL0891 as monotherapy, and in combination with tislelizumab or paclitaxel, to determine the safety and tolerability of increasing doses of BAL0891 in patients with advanced solid… Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Advanced Solid Tumor, TNBC - Triple-Negative Breast Cancer, Gastric Cancer
- What is being tested?
- BAL0891, Tislelizumab and Paclitaxel
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 260 participants
- Where
- 17 sitesin 2 countries
- Study dates
- 14 Dec 2022to 24 Dec 2026
- Phase
- Phase 1
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
1.1. Inclusion criteria: Substudy 1, 2, 3 and Dose expansion Each patient must meet all the following inclusion criteria.
- Informed consent signed by the patient prior to any study-related procedure indicating that they understand the purpose of, and procedures required for, the study, and are willing to participate in the study.
- Male or female aged ≥18 years (or ≥ 19 years according to local regulatory guidelines) at the time of screening.
- Patients with incurable advanced/metastatic solid tumor disease refractory to or intolerant of existing therapy known to provide clinical benefit for their condition. Note: Patients with non-CNS tumors participating during dose escalation may have inactive CNS metastasis, defined as 4 weeks after either brain metastasis resection or radiation, and a) all residual neurological symptoms resolved to grade ≤ 2; b) on stable doses of dexamethasone, if applicable; and c) follow-up imaging shows no new lesions appearing.
- Patients enrolled in Dose Expansion only
- TNBC cohorts i. Must have histologically confirmed breast adenocarcinoma that is unresectable, loco-regional, or metastatic. ii. Must have source data documented pathologically confirmed triple negative breast cancer, defined as both of the following.
- Estrogen receptor (ER) and progesterone receptor (PgR) negative: <1% of tumor cell nuclei are immunoreactive in the presence of evidence that the sample can express ER or PgR (positive intrinsic controls)
- Human epidermal growth factor receptor 2 (HER2) negative as per American Society of Clinical Oncology/College of American Pathologists guidelines
- IHC 0 or 1 fluorescence in situ hybridization (FISH) negative (or equivalent negative test)
- Patients with IHC 2 must have a negative by FISH (or equivalent negative test) iii. Patients with a history of different breast cancer phenotypes (i.e., ER/PgR/HER2 Positive) must obtain pathological confirmation of triple-negative disease in at least one of the current sites of metastasis. iv. Must have progression on or after therapy containing anthracycline and/or a taxane. Subjects must have received anthracycline and/or a taxane based regimen or other chemotherapy / targeted therapy regimen if anthracycline or taxane was contraindicated or another available approved targeted agent was contraindicated. At time of enrolment, patients must have progressed on, be intolerant of, or be ineligible for, all available standard of care therapies with proven benefit.
- GC cohort i. Must have a histologically or cytologically confirmed diagnosis of gastric or gastroesophageal junction adenocarcinoma. ii. Must have progression on or after therapy containing platinum/fluoropyrimidine. Subjects must have received platinum-based chemotherapy or other chemotherapy regimen if platinum-based chemotherapy was contraindicated or another available approved targeted agent unless the targeted agent was contraindicated. At time of enrolment, patients must have progressed on, be intolerant of, or be ineligible for, all available standard of care therapies with proven benefit. iii. Documentation of HER2/neu status. Patients who are HER2/neu-positive must be treated with a HER2/neu inhibitor, and subjects should have progressed on or be intolerant to the targeted therapy or subjects must have received other chemotherapy regimen if HER2/neu inhibitor was contraindicated or another available approved targeted agent unless the targeted agent was contraindicated. At time of enrolment, patients must have progressed on, be intolerant of, or be ineligible for, all available standard of care therapies with proven benefit. iv. Subjects must/should have received no more than 3 lines of prior therapy for the advanced disease (if a subject progressed within 6 months of completing adjuvant therapy, this would count as a prior line of therapy).
- For patients enrolled in Substudy 3 or cohort 3 and 4, if a taxane (i.e., paclitaxel or docetaxel) was administered as part of the previous regimen, PD must have occurred > 12 months from the end of the previous treatment. (Patients who received a taxane in previous treatments without reaching PD may enroll without the 12-month waiting period.)
- Patients enrolled in Dose Expansion only, patient must have undergone a minimum of 1 prior systemic regimen for advanced or metastatic disease. (Korea only, patients must have received the second line standard of care treatment as per the regulations of the respective country. Patients who are unsuitable to receive the standard of care second line treatment will be eligible for enrollment)
- Eastern Cooperative Oncology Group performance status (ECOG PS) 0or-1
- For patients enrolled from DL1.4 of Substudy 1 onwards and for all patients in Substudies 2 and 3 and all four dose expansion cohorts, measurable tumor disease per Response Evaluation Criteria in Solid Tumors 1.1 criteria (RECIST 1.1), i.e., a minimum of one target lesion.
- Adequate organ functions as indicated by the following Screening visit local laboratory values:
- Hemoglobin ≥ 9 g/dL (criterion must be met without erythropoietin dependency and without packed red blood cell transfusion within the last 4 weeks)
- ANC ≥ 2.0 × 109/L; criterion must be met without growth factor (e.g., G-CSF, GM CSF, etc.) administration within the last 2 weeks
- Platelets ≥ 100 × 109/L
- Total bilirubin ≤ 1.5 × ULN
- Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) baseline levels ≤ 1.5 × ULN, with the option for AST/ALT ≤ 3.0 × ULN, or ≤ 5.0 × ULN for patients with liver metastasis, upon accumulating evidence for the absence of liver toxicity in biologically active DLs
- Albumin ≥ 2.8 g/dL
- CLCR ≥ 50 mL/min (as calculated by the Cockcroft-Gault formula), or eGFR ≥ 50 mL/min/1.73 m² (MDRD equation or CKD-EPI equation)
- For women of childbearing potential, negative serum human chorionic gonadotropin (hCG)
- Men/women of child-producing/bearing potential must agree to: avoid impregnating a partner or becoming pregnant, respectively, during the study, and for at least 6 months after the last dose of either investigational drug, and comply with the contraception requirements.
1.2. Inclusion criteria: Substudy 4 Each patient must meet all the following inclusion criteria.
- Informed consent signed by the patient prior to any study-related procedure indicating that they understand the purpose of, and procedures required for, the study, and are willing to participate in the study.
- Male or female aged ≥18 years (or ≥ 19 years according to local regulatory guidelines) at the time of screening.
- Eastern Cooperative Oncology Group performance status (ECOG PS) 0-2.
- Estimated life expectancy of at least 8 weeks
- AML either de novo or secondary as any subtype diagnosed according to the WHO 2022 classification system [except acute promyelocytic leukemia (APL)] who either: Relapse/refractory (R/R) acute myeloid leukemia (AML) defined as those who have also failed or are not appropriate for any approved standard-of-care (SOC) therapies, or hematopoietic stem cell transplant (HSCT) with reappearance of ≥ 5% blasts in the bone marrow.
- Relapsed AML is defined as having 5% or more leukemic blasts in the bone marrow, reappearance of leukemic blasts in peripheral blood (in at least two peripheral blood samples taken at least one week apart), or the development of new extramedullary disease.
- WBC, peripheral blood leukocyte count≤ 25,000/µL and blast count ≤ 25,000/µL prior to initiation of therapy
- Hydroxyurea is allowed during screening and prior to day 1 of study treatment to keep the blast count ≤25,000/µL; hydroxyurea is to be ceased 24 hours prior to study therapy.
- Hydroxyurea may be used for up to 28 days in the initial treatment cycle if needed, to keep the white blood cell (WBC) count ≤25,000/µL. However, no other anti-leukemic treatments, apart from the study drug, are allowed during this period.
- Leukapheresis is allowed to maintain blast count ≤25,000/µL
- Adequate organ functions as indicated by the following Screening visit local laboratory values:
- CLCR ≥ 60 mL/min (as calculated by the Cockcroft-Gault formula), or eGFR ≥ 60 mL/min/1.73 m² (MDRD equation or CKD-EPI equation)
- Total bilirubin ≤ 1.5 × ULN (unless considered due to leukemic organ involvement), or, Direct bilirubin ≤ ULN for subjects with total bilirubin levels > 1.5 ULN
- Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) baseline levels ≤ 3.0 × ULN
- Albumin ≥ 2.5 g/dL
- International Normalized Ratio (INR) or Prothrombin Time (PT) ≤1.5 X ULN unless subject is receiving anticoagulant therapy as long as PT or PTT is within therapeutic range of intended use of anticoagulants
- Activated Partial Thromboplastin Time (aPTT) ≤1.5 X ULN unless subject is receiving anticoagulant therapy as long as PT or PTT is within therapeutic range of intended use of anticoagulants
- Men/women of child-producing/bearing potential must agree to: avoid impregnating a partner or becoming pregnant, respectively, during the study, and for at least 6 months after the last dose of either investigational drug, and comply with the contraception requirements.
Trial locations and contacts
17 sites in 2 countries. Contact the study team or a site near you to ask about taking part.
17 sites in 2 countries
United States11 sites, 9 recruiting
- Recruiting
University of Michigan
Ann Arbor, Michigan, 48109
University of Michigan
- Recruiting
Winship Cancer Institute / Emory University
Atlanta, Georgia, 30322
Winship Cancer Institute / Emory University
- Recruiting
University of Miami Health System
Coral Gables, Florida, 33146
University of Miami Health System
- Completed
Mary Crowley Cancer Research
Dallas, Texas, 75230
- Recruiting
Baylor University Medical Center
Dallas, Texas, 75246
Baylor University Medical Center
- Recruiting
The University of Texas MD Anderson Cancer Center
Houston, Texas, 77030
The University of Texas MD Anderson Cancer Center
- Recruiting
Yale New Haven Hospital
New Haven, Connecticut, 06510
Yale New Haven Hospital
- Recruiting
New York Medicine-New York-Presbyterian Hospital
New York, New York, 10021
New York Medicine-New York-Presbyterian Hospital
- Recruiting
Montefiore Medical Center - Montefiore Hospital
New York, New York, 10467
Montefiore Medical Center - Montefiore Hospital
- Completed
OHSU Knight Cancer Institute
Portland, Oregon, 97239
- Recruiting
Montefiore Medical Center
The Bronx, New York, 10461
Montefiore Medical Center
South Korea6 sites, 6 recruiting
- Recruiting
The Catholic University of Korea, Seoul St. Mary's Hospital
Seoul, 06591
The Catholic University of Korea, Seoul St. Mary's Hospital
- Recruiting
Asan Medical Center
Seoul
Asan Medical Center
- Recruiting
Korean University Anam Hospital
Seoul
Korean University Anam Hospital
- Recruiting
Samsung Medical Center
Seoul
Samsung Medical Center
- Recruiting
Seoul National University Hospital
Seoul
Seoul National University Hospital
- Recruiting
Severance Hospital, Yonsei University Health System
Seoul
Severance Hospital, Yonsei University Health System
About this study
Official title: A Phase 1 Study of BAL0891 as Monotherapy and in Combination With Chemotherapy or Tislelizumab in Patients With Advanced Solid Tumors or Relapsed or Refractory Acute Myeloid Leukemia
This study is a multiple cohort, multicenter, open-label Phase 1 study with dose-escalation substudies investigating intravenous (IV) BAL0891 as monotherapy, and in combination with tislelizumab or paclitaxel, to determine the safety and tolerability of increasing doses of BAL0891 in patients with advanced solid tumors or relapsed or refractory acute myeloid leukemia. An adaptive model-based design will be used to guide the dose escalation. Subject assignment to Substudy 1, 2, 3 and 4 will be finalized following approval from the investigator and sponsor.
The dose-expansion stage will be conducted with the RP2D to further evaluate the preliminary anti-tumor activity, safety, and tolerability in metastatic TNBC and GC.
Read the detailed description
Substudy 1 (monotherapy dose-escalation cohorts) This study will be initiated with enrollment into Substudy 1 and will estimate the safety, tolerability, PK, and PD of increasing doses of BAL0891 in patients with advanced solid tumors. The starting dose will be 5 mg based on the GLP (Good Laboratory Practice) toxicology studies. Dose escalation will comprise a dose range from a dose of 5 mg up to a maximum absolute dose of 480 mg, with eight nominal dose levels (DLs) of 5 / 10 / 20 / 40 / 80 / 160 / 320 / 480 mg. Intra-patient dose escalations are only allowed for patients enrolled in single-patient DL Cohorts 1.1, 1.2, and 1.3. From DL Cohort 1.4 onwards, the projected maximum dose-escalation factor will be two-fold; if the DL cohort investigates an increased dose, dosing of the patients within the cohort must be separated by at least 7 days. For cohorts in which doses are not increased (including backfill enrollment), patients may be enrolled concurrently.
BAL0891 will be administered intravenously (IV) on Day (D) 1 and D8 every 3 weeks (Q3W); for the schedule of assessments of Regimen A. Alternative 21-day or 28-day dosing regimens may be investigated; for the schedule of assessments of Regimens B-D.
Substudies 2 and 3 (dose-escalation cohorts for combination regimens) Enrollment into Substudies 2 and 3 may commence as early as first signs of expected target toxicity and/or efficacy with Regimen A (or an alternative monotherapy regimen) have been observed, or alternatively, once the MTD of BAL0891 monotherapy has been assessed. Patients enrolled into Substudies 2 and 3 will be treated with increasing doses of BAL0891 in combination with tislelizumab or paclitaxel, respectively, and dose escalation of both BAL0891 and tislelizumab/paclitaxel if required will use the same cumulative BLRM-EWOC model as Substudy 1. The starting dose of BAL0891 in combination with tislelizumab or paclitaxel will be a safe DL determined in Substudy 1 but not higher than approximately half the MTD. Backfill enrollment of up to a total of 30 additional patients for both substudies (who may be enrolled concurrently) may be used to better estimate the RP2D for each combination if required.
Substudy 4 (dose escalation cohort for monotherapy in r/r AML) Substudy 4 will evaluate BAL0891 monotherapy in patients with relapsed/refractory AML (r/r AML) using the same BLRM-EWOC model and study design described for Substudy 1. BAL0891 will be administered intravenously on Day 1 and Day 8 every three weeks (Regimen A; see Table 13 for schedule of assessments). Dose exploration will proceed until the highest planned dose level (DL) is determined to be safe and tolerable, or the MTD/RP2D is identified.
Each DL cohort will enroll three patients, with DLT observation required before advancing to the next DL. From DL2 onward, the projected maximum dose-escalation factor will be two-fold, with concurrent enrollment allowed for cohorts without dose increases. Backfill enrollment may be conducted to refine the RP2D and further characterize safety, efficacy and PD.
Part 2 : Dose expansion The commencement of the dose expansion stage will follow the determination of the RP2D achieved during the dose-escalation phase. This stage will consist of four cohorts, each comprising 24 patients who have previously undergone at least one systemic regimen for advanced or metastatic disease. Specifically, two cohorts will be allocated for TNBC, investigating BAL0891 both as a monotherapy and in combination with Paclitaxel. Additionally, two cohorts will be designated for GC, investigating the outcomes of BAL0891 as a monotherapy and in combination with Paclitaxel.
- Conditions
- Advanced Solid Tumor, TNBC - Triple-Negative Breast Cancer, Gastric Cancer, Leukemia Acute Myeloid Leukemia (AML)
- Being tested
- BAL0891, Tislelizumab, Paclitaxel
- Keywords
- carcinoma, paclitaxel, BAL0891, tislelizumab
- Medical subject headings
- Triple Negative Breast Neoplasms, Stomach Neoplasms, Leukemia, Myeloid, Acute, Carcinoma
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
BAL0891Drug
Also called TTK-CS-101
BAL0891 is a dual inhibitor of threonine tyrosine kinase (TTK) and polo-like kinase 1 (PLK1)
TislelizumabCombination product
Tislelizumab a humanized IgG4 anti-PD-1 monoclonal antibody
PaclitaxelCombination product
Also called Taxol
Paclitaxel is a natural product with antitumor activity
| Study group | Role | What they receive |
|---|---|---|
| Part 1: Substudy 1, Dose-escalation substudy of BAL0891 monotherapy | Experimental | Increasing doses of BAL0891 will be administered IV on D1 and D8 Q3W (Regimen A). BAL0891 will be investigated in a dose range of 5-480 mg with Regimen A. Optionally, and based on cumulative safety, PK, and PD data, BAL0891 may be administered on D1 Q3W (Regimen B), D1 and D15 Q4W (Regimen C), or on D1, D8, and D15 Q4W (Regimen D). Receives: Drug: BAL0891 |
| Part 1: Substudy 2, Dose-escalation substudy of BAL0891 in combination with tislelizumab | Experimental | Increasing doses of BAL0891 will be administrated IV on D1 and D15 with tislelizumab administration on D8 Q3W. The starting dose of BAL0891 for combination will be at approximately 50% of the BAL0891 monotherapy MTD determined in Substudy 1 and tislelizumab dose will be 200mg IV. Receives: Drug: BAL0891; Combination Product: Tislelizumab |
| Part 1: Substudy 3, Dose-escalation substudy of BAL0891 in combination with paclitaxel | Experimental | Paclitaxel will be dosed at 70 mg/m2 on D1, D8, and D15 Q4W, with an option to use 80 mg/m2 (either instead of, or after exploring, 70 mg/m2) if the cumulative data collected at that time support a higher dose of paclitaxel. Receives: Drug: BAL0891; Combination Product: Paclitaxel |
| Part 2 : Dose expansion, cohorts 1 TNBC (BAL0891 monotherapy) | Experimental | BAL0891 will be administered intravenously on D1 and D8, Q3W for cohorts 1. The investigation will focus on the RP2D determined during the dose escalation phase of the study. Specifically, cohorts 1 will utilize the RP2D established in substudy 1 of the dose escalation phase. Receives: Drug: BAL0891 |
| Part 2 : Dose expansion, cohorts 2 GC (BAL0891 monotherapy) | Experimental | BAL0891 will be administered intravenously on D1 and D8, Q3W for cohorts 2. The investigation will focus on the RP2D determined during the dose escalation phase of the study. Specifically, cohorts 2 will utilize the RP2D established in substudy 1 of the dose escalation phase. Receives: Drug: BAL0891 |
| Part 2 : Dose expansion, cohorts 3 TNBC (BAL0891 + Paclitaxel) | Experimental | BAL0891 will be administered intravenously on D1 and D15, Q4W for cohorts 3 . The investigation will focus on the RP2D determined during the dose escalation phase of the study. Specifically, cohorts 3 will utilize the RP2D established in substudy 3 of the dose escalation phase. Receives: Drug: BAL0891; Combination Product: Paclitaxel |
| Part 2 : Dose expansion, cohorts 4 GC (BAL0891 + Paclitaxel) | Experimental | BAL0891 will be administered intravenously on D1 and D15, Q4W for cohorts 4. The investigation will focus on the RP2D determined during the dose escalation phase of the study. Specifically, cohorts 4 will utilize the RP2D established in substudy 3 of the dose escalation phase. Receives: Drug: BAL0891; Combination Product: Paclitaxel |
| Part 1: Substudy 4, Dose-escalation substudy of BAL0891 monotherapy in r/r AML | Experimental | BAL0891 will be administered intravenously on Day 1 and Day 8 every three weeks (Regimen A). Dose exploration will proceed until the highest planned dose level (DL) is determined to be safe and tolerable, or the MTD/RP2D is identified. Receives: Drug: BAL0891 |
What is being measured
The primary outcome is the main question the study is designed to answer.
Part 1: Number of Participants With Adverse Events as a Measure of Safety and Tolerability
Safety is collected through summaries of AE(Adverse Event)s, safety laboratory evaluations, PK evaluations, physical examinations, vital signs, and ECGs using CTCAE v5.0.
Measured: After first dose, up to 2 years
Part 1: Number of Participants With the DLT (Dose-limiting toxicity)s as a Measure of maximum tolerated dose (MTD) and/or the recommended Phase 2 dose (RP2D)
DLTs are collected through BLRM-EWOC.
Measured: After first dose and within 7 days of End of Treatment, up to 2 years
Part 2: Overall response rate (ORR) for all subjects
The proportion of patients with confirmed complete response (CR) or partial response (PR) by RECIST 1.1/iRECIST (substudy 2 only) during the dose expansion phase.
Measured: Every 3 months (±14 days) after first dose, up to 2 years
Secondary outcomes (17)
Part 1: Pharmacokinetics (PK) parameters for all subjects
The area under the plasma concentration-time curve (AUC) by PK Sampling
Measured: Within 7 days of End of Treatment, up to 2 years
Part 1: Absolute neutrophil count (ANC) for all subjects
Duration of neutropenia by PD Sampling
Measured: Within 7 days of End of Treatment, up to 2 years
Part 1, 2: Overall response rate (ORR) for all subjects
The proportion of patients with confirmed complete response (CR) or partial response (PR) by RECIST 1.1
Measured: Every 3 months (±14 days) after first dose, up to 2 years
Part 1, 2: Disease control rate (DCR) for all subjects
The proportion of patients with confirmed CR, PR or stable disease (SD) by RECIST 1.1
Measured: Within 7 days of End of Treatment, up to 2 years
Part 1, 2: Progression-free survival (PFS) for all subjects
Measured from patient enrollment to disease progression date
Measured: Within 7 days of End of Treatment, up to 2 years
Part 1, 2: Overall survival (OS) for all subjects
Measured from from patient enrollment to time of death
Measured: Within 7 days of End of Treatment, up to 2 years
Part 2: Safety evaluations for all subjects
Safety evaluations is focusing on key clinical evlauations such treatment-emergent adverse events (TEAE) using CTCAE v5.0.
Measured: After first dose, up to 2 years
Part 1: Efficacy Endpoints CR + CRh Rate (Substudy 4)
Proportion of patients achieving Complete Remission (CR) or CR with partial hematologic recovery (CRh) per European LeukemiaNet (ELN) 2022 guidelines.
Measured: Up to 2 years
Part 1: Efficacy Endpoints Duration of Remission (DoR) (Substudy 4)
Time from first documented CR/CRh until relapse or death.
Measured: Up to 2 years
Part 1: Efficacy Endpoints Transfusion Independence (TI) (Substudy 4)
Proportion of patients achieving red blood cell (RBC) and platelet transfusion independence for ≥56 consecutive days.
Measured: Up to 2 years
Part 1: Efficacy Endpoints CR/CRh without Measurable Residual Disease (MRD) (Substudy 4)
Proportion of patients achieving CR/CRh and MRD negativity.
Measured: Up to 2 years
Part 1: Efficacy Endpoints Composite Complete Remission (CRc) Rate (Substudy 4)
Proportion of patients achieving CR, CRh, or CR with incomplete hematologic recovery (CRi).
Measured: Up to 2 years
Part 1: Efficacy Endpoints Overall Response Rate (ORR) (Substudy 4)
Proportion of patients achieving CR, CRh, CRi, or Partial Remission (PR).
Measured: Up to 2 years
Part 1: Efficacy Endpoints Overall Survival (OS) (Substudy 4)
Time from first dose of BAL0891 to death from any cause.
Measured: Up to 2 years
Part 1: Efficacy Endpoints Event-Free Survival (EFS) (Substudy 4)
Time from first dose of BAL0891 to disease progression, relapse, or death.
Measured: Up to 2 years
Part 1: Efficacy Endpoints Time to Response (TTR) (Substudy 4)
Time from first dose of BAL0891 to first documented response.
Measured: Up to 2 years
Part 1: QTcF Interval Analysis
Analysis of QTcF interval data collected during BAL0891 monotherapy and the relationship between BAL0891 exposure and QTcF interval prolongation.
Measured: From first dose to 30 days post last dose
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted15 Mar 2023
- Study start14 Dec 2022
- Primary completion24 Dec 2026 (estimated)
- Study completion24 Dec 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Advanced Solid TumorStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 1
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Sequential
- Masking
- None (open label)
- Enrolment
- 260 participants (estimated)
Sponsor and investigators
- Lead sponsor
- SillaJen, Inc.
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- SillaJen Inc., Study director, SillaJen, Inc.
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05768932
- Sponsor's protocol ID
- TTK-CS-101
- Status last verified
- Jun 2026
- First submitted
- 29 Jan 2023
- Last updated
- 15 Jun 2026
- Results posted
- No
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 15 Jun 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Phase 1 Study of BAL0891 as Monotherapy and in Combination With Chemotherapy or Tislelizumab in Patients With Advanced Solid Tumors or Relapsed or Refractory Acute Myeloid Leukemia
- ClinicalTrials.gov ID
- NCT05768932
- Acronym / sponsor ID
- TTK-CS-101
- Conditions
- Advanced Solid Tumor, TNBC - Triple-Negative Breast Cancer, Gastric Cancer, Leukemia Acute Myeloid Leukemia (AML)
- Keywords
- carcinoma, paclitaxel, BAL0891, tislelizumab
- Phase
- Phase 1
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 260 participants (estimated)
- Lead sponsor
- SillaJen, Inc.Industry (pharma, biotech, devices)
- Study start
- 14 Dec 2022 (actual)
- Primary completion
- 24 Dec 2026 (estimated)
- Study completion
- 24 Dec 2026 (estimated)
- First posted
- 15 Mar 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study is a multiple cohort, multicenter, open-label Phase 1 study with dose-escalation substudies investigating intravenous (IV) BAL0891 as monotherapy, and in combination with tislelizumab or paclitaxel, to determine the safety and tolerability of increasing doses of BAL0891 in patients with advanced solid tumors or relapsed or refractory acute myeloid leukemia. An adaptive model-based design will be used to guide the dose escalation. Subject assignment to Substudy 1, 2, 3 and 4 will be finalized following approval from the investigator and sponsor.
The dose-expansion stage will be conducted with the RP2D to further evaluate the preliminary anti-tumor activity, safety, and tolerability in metastatic TNBC and GC.
Detailed description
Substudy 1 (monotherapy dose-escalation cohorts) This study will be initiated with enrollment into Substudy 1 and will estimate the safety, tolerability, PK, and PD of increasing doses of BAL0891 in patients with advanced solid tumors. The starting dose will be 5 mg based on the GLP (Good Laboratory Practice) toxicology studies. Dose escalation will comprise a dose range from a dose of 5 mg up to a maximum absolute dose of 480 mg, with eight nominal dose levels (DLs) of 5 / 10 / 20 / 40 / 80 / 160 / 320 / 480 mg. Intra-patient dose escalations are only allowed for patients enrolled in single-patient DL Cohorts 1.1, 1.2, and 1.3. From DL Cohort 1.4 onwards, the projected maximum dose-escalation factor will be two-fold; if the DL cohort investigates an increased dose, dosing of the patients within the cohort must be separated by at least 7 days. For cohorts in which doses are not increased (including backfill enrollment), patients may be enrolled concurrently.
BAL0891 will be administered intravenously (IV) on Day (D) 1 and D8 every 3 weeks (Q3W); for the schedule of assessments of Regimen A. Alternative 21-day or 28-day dosing regimens may be investigated; for the schedule of assessments of Regimens B-D.
Substudies 2 and 3 (dose-escalation cohorts for combination regimens) Enrollment into Substudies 2 and 3 may commence as early as first signs of expected target toxicity and/or efficacy with Regimen A (or an alternative monotherapy regimen) have been observed, or alternatively, once the MTD of BAL0891 monotherapy has been assessed. Patients enrolled into Substudies 2 and 3 will be treated with increasing doses of BAL0891 in combination with tislelizumab or paclitaxel, respectively, and dose escalation of both BAL0891 and tislelizumab/paclitaxel if required will use the same cumulative BLRM-EWOC model as Substudy 1. The starting dose of BAL0891 in combination with tislelizumab or paclitaxel will be a safe DL determined in Substudy 1 but not higher than approximately half the MTD. Backfill enrollment of up to a total of 30 additional patients for both substudies (who may be enrolled concurrently) may be used to better estimate the RP2D for each combination if required.
Substudy 4 (dose escalation cohort for monotherapy in r/r AML) Substudy 4 will evaluate BAL0891 monotherapy in patients with relapsed/refractory AML (r/r AML) using the same BLRM-EWOC model and study design described for Substudy 1. BAL0891 will be administered intravenously on Day 1 and Day 8 every three weeks (Regimen A; see Table 13 for schedule of assessments). Dose exploration will proceed until the highest planned dose level (DL) is determined to be safe and tolerable, or the MTD/RP2D is identified.
Each DL cohort will enroll three patients, with DLT observation required before advancing to the next DL. From DL2 onward, the projected maximum dose-escalation factor will be two-fold, with concurrent enrollment allowed for cohorts without dose increases. Backfill enrollment may be conducted to refine the RP2D and further characterize safety, efficacy and PD.
Part 2 : Dose expansion The commencement of the dose expansion stage will follow the determination of the RP2D achieved during the dose-escalation phase. This stage will consist of four cohorts, each comprising 24 patients who have previously undergone at least one systemic regimen for advanced or metastatic disease. Specifically, two cohorts will be allocated for TNBC, investigating BAL0891 both as a monotherapy and in combination with Paclitaxel. Additionally, two cohorts will be designated for GC, investigating the outcomes of BAL0891 as a monotherapy and in combination with Paclitaxel.
Study design
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Sequential
- Masking
- None (open label)
- Number of arms
- 8
| Arm | Type | Receives |
|---|---|---|
| Part 1: Substudy 1, Dose-escalation substudy of BAL0891 monotherapy | Experimental | Drug: BAL0891Increasing doses of BAL0891 will be administered IV on D1 and D8 Q3W (Regimen A). BAL0891 will be investigated in a dose range of 5-480 mg with Regimen A. Optionally, and based on cumulative safety, PK, and PD data, BAL0891 may be administered on D1 Q3W (Regimen B), D1 and D15 Q4W (Regimen C), or on D1, D8, and D15 Q4W (Regimen D). |
| Part 1: Substudy 2, Dose-escalation substudy of BAL0891 in combination with tislelizumab | Experimental | Drug: BAL0891, Combination Product: TislelizumabIncreasing doses of BAL0891 will be administrated IV on D1 and D15 with tislelizumab administration on D8 Q3W. The starting dose of BAL0891 for combination will be at approximately 50% of the BAL0891 monotherapy MTD determined in Substudy 1 and tislelizumab dose will be 200mg IV. |
| Part 1: Substudy 3, Dose-escalation substudy of BAL0891 in combination with paclitaxel | Experimental | Drug: BAL0891, Combination Product: PaclitaxelPaclitaxel will be dosed at 70 mg/m2 on D1, D8, and D15 Q4W, with an option to use 80 mg/m2 (either instead of, or after exploring, 70 mg/m2) if the cumulative data collected at that time support a higher dose of paclitaxel. |
| Part 2 : Dose expansion, cohorts 1 TNBC (BAL0891 monotherapy) | Experimental | Drug: BAL0891BAL0891 will be administered intravenously on D1 and D8, Q3W for cohorts 1. The investigation will focus on the RP2D determined during the dose escalation phase of the study. Specifically, cohorts 1 will utilize the RP2D established in substudy 1 of the dose escalation phase. |
| Part 2 : Dose expansion, cohorts 2 GC (BAL0891 monotherapy) | Experimental | Drug: BAL0891BAL0891 will be administered intravenously on D1 and D8, Q3W for cohorts 2. The investigation will focus on the RP2D determined during the dose escalation phase of the study. Specifically, cohorts 2 will utilize the RP2D established in substudy 1 of the dose escalation phase. |
| Part 2 : Dose expansion, cohorts 3 TNBC (BAL0891 + Paclitaxel) | Experimental | Drug: BAL0891, Combination Product: PaclitaxelBAL0891 will be administered intravenously on D1 and D15, Q4W for cohorts 3 . The investigation will focus on the RP2D determined during the dose escalation phase of the study. Specifically, cohorts 3 will utilize the RP2D established in substudy 3 of the dose escalation phase. |
| Part 2 : Dose expansion, cohorts 4 GC (BAL0891 + Paclitaxel) | Experimental | Drug: BAL0891, Combination Product: PaclitaxelBAL0891 will be administered intravenously on D1 and D15, Q4W for cohorts 4. The investigation will focus on the RP2D determined during the dose escalation phase of the study. Specifically, cohorts 4 will utilize the RP2D established in substudy 3 of the dose escalation phase. |
| Part 1: Substudy 4, Dose-escalation substudy of BAL0891 monotherapy in r/r AML | Experimental | Drug: BAL0891BAL0891 will be administered intravenously on Day 1 and Day 8 every three weeks (Regimen A). Dose exploration will proceed until the highest planned dose level (DL) is determined to be safe and tolerable, or the MTD/RP2D is identified. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| BAL0891Also: TTK-CS-101BAL0891 is a dual inhibitor of threonine tyrosine kinase (TTK) and polo-like kinase 1 (PLK1) | Drug | Part 1: Substudy 1, Dose-escalation substudy of BAL0891 monotherapy, Part 1: Substudy 2, Dose-escalation substudy of BAL0891 in combination with tislelizumab, Part 1: Substudy 3, Dose-escalation substudy of BAL0891 in combination with paclitaxel, Part 1: Substudy 4, Dose-escalation substudy of BAL0891 monotherapy in r/r AML, Part 2 : Dose expansion, cohorts 1 TNBC (BAL0891 monotherapy), Part 2 : Dose expansion, cohorts 2 GC (BAL0891 monotherapy), Part 2 : Dose expansion, cohorts 3 TNBC (BAL0891 + Paclitaxel), Part 2 : Dose expansion, cohorts 4 GC (BAL0891 + Paclitaxel) |
| TislelizumabTislelizumab a humanized IgG4 anti-PD-1 monoclonal antibody | Combination product | Part 1: Substudy 2, Dose-escalation substudy of BAL0891 in combination with tislelizumab |
| PaclitaxelAlso: TaxolPaclitaxel is a natural product with antitumor activity | Combination product | Part 1: Substudy 3, Dose-escalation substudy of BAL0891 in combination with paclitaxel, Part 2 : Dose expansion, cohorts 3 TNBC (BAL0891 + Paclitaxel), Part 2 : Dose expansion, cohorts 4 GC (BAL0891 + Paclitaxel) |
Primary outcome
Part 1: Number of Participants With Adverse Events as a Measure of Safety and Tolerability
Time frame: After first dose, up to 2 years
Safety is collected through summaries of AE(Adverse Event)s, safety laboratory evaluations, PK evaluations, physical examinations, vital signs, and ECGs using CTCAE v5.0.
Part 1: Number of Participants With the DLT (Dose-limiting toxicity)s as a Measure of maximum tolerated dose (MTD) and/or the recommended Phase 2 dose (RP2D)
Time frame: After first dose and within 7 days of End of Treatment, up to 2 years
DLTs are collected through BLRM-EWOC.
Part 2: Overall response rate (ORR) for all subjects
Time frame: Every 3 months (±14 days) after first dose, up to 2 years
The proportion of patients with confirmed complete response (CR) or partial response (PR) by RECIST 1.1/iRECIST (substudy 2 only) during the dose expansion phase.
17 secondary outcomes
Part 1: Pharmacokinetics (PK) parameters for all subjects
Time frame: Within 7 days of End of Treatment, up to 2 years
Part 1: Absolute neutrophil count (ANC) for all subjects
Time frame: Within 7 days of End of Treatment, up to 2 years
Part 1, 2: Overall response rate (ORR) for all subjects
Time frame: Every 3 months (±14 days) after first dose, up to 2 years
Part 1, 2: Disease control rate (DCR) for all subjects
Time frame: Within 7 days of End of Treatment, up to 2 years
Part 1, 2: Progression-free survival (PFS) for all subjects
Time frame: Within 7 days of End of Treatment, up to 2 years
Part 1, 2: Overall survival (OS) for all subjects
Time frame: Within 7 days of End of Treatment, up to 2 years
Part 2: Safety evaluations for all subjects
Time frame: After first dose, up to 2 years
Part 1: Efficacy Endpoints CR + CRh Rate (Substudy 4)
Time frame: Up to 2 years
Part 1: Efficacy Endpoints Duration of Remission (DoR) (Substudy 4)
Time frame: Up to 2 years
Part 1: Efficacy Endpoints Transfusion Independence (TI) (Substudy 4)
Time frame: Up to 2 years
Part 1: Efficacy Endpoints CR/CRh without Measurable Residual Disease (MRD) (Substudy 4)
Time frame: Up to 2 years
Part 1: Efficacy Endpoints Composite Complete Remission (CRc) Rate (Substudy 4)
Time frame: Up to 2 years
Part 1: Efficacy Endpoints Overall Response Rate (ORR) (Substudy 4)
Time frame: Up to 2 years
Part 1: Efficacy Endpoints Overall Survival (OS) (Substudy 4)
Time frame: Up to 2 years
Part 1: Efficacy Endpoints Event-Free Survival (EFS) (Substudy 4)
Time frame: Up to 2 years
Part 1: Efficacy Endpoints Time to Response (TTR) (Substudy 4)
Time frame: Up to 2 years
Part 1: QTcF Interval Analysis
Time frame: From first dose to 30 days post last dose
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 15 Jun 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
SillaJen Inc. study director
SillaJen, Inc.
17 sites in 2 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 1 study testing BAL0891, Tislelizumab and Paclitaxel in people with Advanced Solid Tumor and TNBC - Triple-Negative Breast Cancer, run by SillaJen, Inc. at 17 sites in 2 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 15 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 17 sites in United States, South Korea. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact SillaJen Inc. (02-368-2600, patient_inquiry@sillajen.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Part 1: Number of Participants With Adverse Events as a Measure of Safety and Tolerability (time frame: After first dose, up to 2 years). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Jun 2026.