CLINICAL TRIAL / NCT04742959
Study of TT-00420 (Tinengotinib) Tablet as Monotherapy and Combination Therapy in Patients With Advanced Solid Tumors
- Interventional
- Recruiting
- NCT04742959
Contact Information
A Phase Ib/II, Multicenter, Open-Label Study of TT-00420 Tablet, as Monotherapy or in Combination Regimens, in Patients With Advanced Solid Tumors
This is a Phase Ib/II, multicenter, open-label study to evaluate the safety and preliminary efficacy of TT-00420 tablet, as monotherapy or in combination regimens, in patients with advanced solid tumors.
Study consists of three arms, Arm A is a Phase Ib/II study of TT-00420 tablet
monotherapy, Arm B is a Phase Ib/II study of TT-00420 tablet in combination with
nab-paclitaxel (Abraxane®) and Arm C is a PK run-in study of TT-00420 tablet.
Arm A: TT-00420 Tablet Monotherapy Phase Ib will enroll patients with preferred
indications including metastatic cholangiocarcinoma, HER2-negative breast cancer
including TNBC, bladder cancer, small cell lung cancer, prostate cancer, thyroid cancer,
sarcoma, gastric cancer, gallbladder cancer and other advanced solid tumors to receive
TT-00420 monotherapy. Based on preliminary efficacy results, Phase II will enroll
additional patients in select indications to evaluate the efficacy of TT-00420
monotherapy.
Arm B: TT-00420 tablet in combination with nab-paclitaxel (Abraxane®) Arm B will enroll
patients with metastatic HER2-negative breast cancers, including triple-negative breast
cancer (TNBC). Phase Ib will be a dose escalation study of TT-00420 in combination with
nab-paclitaxel, guided by 3+3 design, to determine a Recommended Phase 2 Dose (RP2D).
Phase II will enroll additional patients with metastatic HER2-negative breast cancers to
further evaluate the efficacy of the combination regimen.
Arm C: PK Run-in Study of TT-00420 Tablet Arm C will enroll patients with preferred
indications including cholangiocarcinoma, TNBC/HER2- negative breast cancer, prostate
cancer, sarcoma, hepatocellular carcinoma (HCC), bladder cancer, small cell lung cancer,
thyroid cancer, gastric cancer, gallbladder cancer and other advanced solid tumors to
receive TT-00420 monotherapy administered as once daily (q.d.) or twice daily (b.i.d.).
Gender
All
Age Group
18 Years and up
Accepting Healthy Volunteers
No
Inclusion Criteria:
1. ≥ 18 years of age
2. Histopathological or cytologically documented locally advanced or metastatic solid
tumors who have no available standard therapeutic treatment options
3. At least one measurable lesion as defined by RECIST V1.1 criteria for solid tumors
4. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
5. Adequate organ function confirmed at screening and within 10 days of initiating
treatment, as evidenced by:
- Absolute neutrophil count (ANC) ≥ 1.5 x 10^9/L
- Hemoglobin (Hgb) ≥ 8 g/dl
- Platelets (plt) ≥ 75 x 10^9/L
- AST/SGOT and ALT/SGPT ≤ 2.5 x Upper Limit of Normal (ULN) or ≤ 5.0 x ULN if
liver metastases are present
- Total bilirubin ≤ 1.5 x ULN
- Calculated creatinine clearance ≥ 50 mL/min (Cockcroft Gault formula)
6. Negative pregnancy test within 72 hours before starting study treatment in all
premenopausal women and women < 12 months after the onset of menopause
7. Must agree to take sufficient contraceptive methods to avoid pregnancy during the
study and until at least 6 months after ceasing study treatment
8. Able to sign informed consent and comply with the protocol
Exclusion Criteria:
1. Women who are pregnant or lactating
2. Women of child-bearing potential (WOCBP) who do not use adequate birth control
3. Patients with any hematologic malignancy, including leukemia (any form), lymphoma,
and multiple myeloma
4. Patients with a history of primary central nervous system tumors or carcinomatous
meningitis.
5. Patients with the following mood disorders as judged by the Investigator or a
psychiatrist:
- Medically documented history of or active major depressive episode, bipolar
disorder (I or II), obsessive-compulsive disorder, schizophrenia; a history of
suicidal attempt or ideation, or homicidal ideation (immediate risk of doing
harm to others)
- ≥ CTCAE grade 3 anxiety
6. Impaired cardiac function or significant diseases, including but not limited to any
of the following:
- left ventricular ejection fraction (LVEF) < 45% as determined by multigated
acquisition (MUGA) scan or echocardiogram (ECHO)
- Congenital long QT syndrome
- QTcF ≥ 480 msec on screening ECG
- Unstable angina pectoris ≤ 3 months prior to starting study drug
- Acute myocardial infarction ≤ 3 months prior to starting study drug
7. Patients with:
- unresolved diarrhea ≥ CTCAE grade 2, or
- impairment of gastrointestinal (GI) function, or
- GI disease that may significantly alter the absorption of TT-00420
8. Other concurrent severe and/or uncontrolled concomitant medical conditions (e.g.,
uncontrolled hypertension, uncontrolled hypertriglyceridemia, or active or
uncontrolled infection) that could cause unacceptable safety risks or compromise
compliance with the protocol
9. Patients who have received chemotherapy, targeted therapy, or immunotherapy ≤ 4
weeks (6 weeks for nitrosourea or mitomycin-C) prior to starting study drug or who
have not recovered from side effects of such therapy
10. Patients who have received wide field radiotherapy ≤ 4 weeks or limited field
radiation for palliation ≤ 2 weeks prior to starting study drug or who have not
recovered from side effects of such therapy
11. Patients who have undergone major surgery ≤ 4 weeks prior to starting study drug or
who have not recovered from side effects of such therapy
12. Patients who have been treated with any hematopoietic colony-stimulating growth
factors (e.g., G-CSF, GM-CSF) ≤ 4 weeks prior to starting study drug.
13. Patients who are currently receiving treatment with therapeutic doses of warfarin
sodium or any other coumarin-derivative anticoagulants
14. Patients who have received systemic corticosteroids ≤ 2 weeks prior to starting
study drug or who have not recovered from the side effects of such treatment.
15. Patients who are currently receiving treatment with strong CYP3A inhibitors or
inducers ≤ 2 weeks prior to starting study drug.
16. Known diagnosis of human immunodeficiency virus (HIV) infection (HIV testing is not
mandatory; patients with well controlled HIV might be enrolled)
17. Known history of active infection with Hepatitis B or Hepatitis C
18. Has received a live-virus vaccination within 30 days of planned first dose
19. Inability to swallow or tolerate oral medication
20. Has a history or current evidence of any condition, therapy, or laboratory
abnormality that, in the opinion of the investigator, might confound the results of
the trial, interfere with the patient's safe participation and compliance in the
trial.
- Bladder Cancer
- Breast Cancer
- Cholangiocarcinoma
- Gallbladder Cancer
- Gastric Cancer
- Prostate Cancer
- Solid Tumors
- Thyroid Cancer