Study of DCC-3014 in Patients With Advanced Tumors and Tenosynovial Giant Cell Tumor

Inclusion Criteria

Dose Escalation Phase:

   1. Patients ≥18 years of age

   2. Patients must have:

      1. advanced malignant solid tumors; or

      2. symptomatic TGCT for which surgical resection is not an option (tumor biopsy to
      confirm diagnosis required if no histology/pathology available at screening)

   3. Malignant solid tumor patients only: Able to provide a tumor tissue sample

   4. Must have 1 measurable lesion according to RECIST Version 1.1

   5. Malignant solid tumor patients only: Must have ECOG performance status of 0-1

   6. Adequate organ and bone marrow function

   7. If a female of childbearing potential, must have a negative pregnancy test prior to
   enrollment and agree to follow the contraception requirements.

   8. Must provide signed consent to participate in the study and is willing to comply with
   study-specific procedures.

Expansion Phase (Cohorts A and B)

   1. Patients ≥18 years of age

   2. Patients must have symptomatic TGCT for which surgical resection is not an option
   (tumor biopsy to confirm diagnosis required if no histology/pathology available at
   screening)

   a) Expansion Cohort B: patients must have prior systemic treatment with anti-CSF1 or
   anti-CSF1R therapy, with the exception of imatinib or nilotinib

   3. Adequate organ and bone marrow function

   4. Must have at least 1 measurable lesion according to RECIST Version 1.1

   5. If a female of childbearing potential, must have a negative pregnancy test prior to
   enrollment and agree to follow the contraception requirements.

   6. Must provide signed consent to participate in the study and is willing to comply with
   study-specific procedures.

Exclusion Criteria

Dose Escalation Phase:

   1. Received anticancer therapy or therapy for TGCT, including investigational therapy,
   within 2 weeks or 28 days for therapies with half-life (t1/2) longer than 3 days prior
   to the administration of study drug.

   2. Unresolved toxicity (Grade >1 or baseline) from previous anticancer therapy or TGCT
   therapy, excluding alopecia.

   3. Known active CNS metastases.

   4. History or presence of clinically relevant cardiovascular abnormalities.

   5. Systemic arterial or venous thrombotic or embolic events.

   6. QT interval corrected by Fridericia's formula (QTcF) >450 ms in males or >470 ms in
   females or history of long QT syndrome.

   7. Left ventricular ejection fraction (LVEF) <50%.

   8. Concurrent treatment with proton-pump inhibitor(s).

   9. Major surgery within 2 weeks of the first dose of study drug.

10. Malabsorption syndrome or other illness that could affect oral absorption.

11. Known human immunodeficiency virus, active hepatitis B, active hepatitis C, or active
   mycobacterium tuberculosis infection.

12. If female, the patient is pregnant or lactating.

13. Known allergy or hypersensitivity to any component of the study drug.

14. Any other clinically significant comorbidities.

Expansion Phase (Cohorts A and B)

   1. Expansion Cohort A: received systemic therapy targeting CSF1 or CSF1R; previous
   therapy with imatinib and nilotinib is allowed.

   2. Expansion Cohort B: discontinued systemic therapy targeting anti-CSF1 or anti-CSF1R
   due to drug-induced liver injury.

   3. Treatment with therapy for TGCT, including investigational therapy, within 2 weeks or
   28 days for therapies with a t1/2 longer than 3 days prior to the administration of
   the study drug.

   4. Known metastatic TGCT or other active cancer that requires concurrent treatment.

   5. QT interval corrected by Fridericia's formula (QTcF) >450 ms in males or >470 ms in
   females or history of long QT syndrome.

   6. Left ventricular ejection fraction (LVEF) <55%.

   7. Concurrent treatment with proton-pump inhibitor(s).

   8. Major surgery within 2 weeks of the first dose of study drug.

   9. Any clinically significant comorbidities

10. Malabsorption syndrome or other illness that could affect oral absorption.

11. Known human immunodeficiency virus (HIV), active or chronic hepatitis B, active or
   chronic hepatitis C, or active mycobacterium tuberculosis infection.

12. If female, the patient is pregnant or lactating.

13. Known allergy or hypersensitivity to any component of the study drug.

14. Contraindication for MRI

15. Active liver or biliary disease, including evidence of fatty liver, nonalcoholic
   steatohepatitis (NASH), or cirrhosis