A Study of NB003 in Patients With Advanced Malignancies

Inclusion Criteria:

   1. Males or females of any race ≥18 years age.

   2. Histologically-confirmed diagnosis of unresectable, relapsed or metastatic GIST or
   other advanced malignancies.

      1. For dose escalation phase:

         - GIST patients must have progressed on or had an intolerability to imatinib
         and other SoCs or refused other SoCs.

         - Patients with an advanced solid tumor other than GIST must have relapsed or
         had refractory disease without an available effective therapy and harbor KIT
         or PDGFRα gene alterations (central laboratory confirmation is not required
         for screening).

      2. For dose expansion phase:

   Cohort 1: GIST patients with KIT or PDGFRα gene mutations, must have progressed on or
   been intolerant to at least imatinib, sunitinib, regorafenib and ripretinib (≥ fifth
   line therapy setting); Cohort 2a: GIST patients with KIT or PDGFRα gene mutations,
   must have progressed on or been intolerant to imatinib and sunitinib, and who have not
   received additional systemic therapy for advanced GIST (third line therapy setting);
   Cohort 2b: GIST patients with KIT or PDGFRα gene mutations, must have progressed on or
   been intolerant to imatinib, sunitinib and regorafenib, and who have not received
   additional systemic therapy for advanced GIST (forth line therapy setting); Cohort 3:
   GIST patients with KIT or PDGFRα gene mutations, must have progressed on or been
   intolerant to imatinib and have not received additional systemic therapy for advanced
   GIST (second line therapy setting); Cohort 4: GIST patients with PDGFRα exon 18
   mutation and must have progressed on or been intolerant to avapritinib; in the
   countries/regions where avapritinib is not SoC, avapritinib-naïve patients can be
   enrolled; Cohort 5: Unresectable or metastatic melanoma patients with demonstrated
   evidence for KIT gene mutation and/or amplification, must have progressed on or been
   intolerant to SoCs; Cohort 6: Patients with other advanced malignancies other than
   GIST or melanoma which must be relapsed or refractory without an available effective
   therapy and harbor KIT or PDGFRα gene alterations.

   3. For dose expansion phase: at least one measurable lesion per RECIST v1.1/mRECIST.

   4. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.

   5. Life expectancy ≥ 12 weeks.

   6. Adequate organ and marrow function.

   7. Tumor sample collection is required.

Exclusion Criteria:

   1. Prior anti-cancer therapy within 2 weeks or at least 5 half-lives, whichever is
   longer, up to a maximum wash-out period of 21 days prior to the initiation of study
   drug administration.

   2. Major surgery within 4 weeks of the first dose.

   3. Radiotherapy with a limited field of radiation for palliation within 1 week prior to
   the first dose, with the exception as defined.

   4. Patients currently receiving medications or herbal supplements known to be strong
   inhibitors or inducers of CYP3A4.

   5. Patients currently receiving acid-reducing agents and are unable to stop use at least
   2 weeks prior to the first dose.

   6. Any known active central nervous system metastases and/or carcinomatous meningitis.
   Active infection including hepatitis B, hepatitis C, and HIV.

   7. Any other clinically significant comorbidities, such as uncontrolled pulmonary
   disease, active infection, uncontrolled pericardial effusion, uncontrolled pleural
   effusion, or any other conditions, which in the judgment of Investigator, could
   compromise compliance with the protocol, interfere with the interpretation of study
   results, or predispose the patient to safety risks.

   8. Any evidence of severe or uncontrolled systemic diseases which in the Investigator's
   opinion makes it undesirable for the patient to participate in the trial or which
   would jeopardize compliance with the protocol.