OMT-111 for Terminal Stage Solid Tumors

Inclusion Criteria:

* Breast Cancer

  1. Female at least 18 years old or older at the time of informed consent
  2. Histologically or cytologically confirmed triple negative ductal adenocarcinoma of breast
  3. Patients who have visceral metastatic lesions not amenable by resection or radiotherapy (e.g., multiple visceral lesions)
  4. ECOG PS (Eastern Cooperative Oncology Group Performance Status): 0-2
  5. Patients with a life expectancy ≥ 12 weeks as judged by the investigator
  6. At least one measurable lesion or evaluable lesion defined by the Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1
* Pancreatic Cancer

  1. Male or female at least 18 years old or older at the time of informed consent
  2. Histologically or cytologically confirmed adenocarcinoma of pancreas
  3. Patients who have advanced or metastatic lesions not amenable by resection or radiotherapy
  4. ECOG PS (Eastern Cooperative Oncology Group Performance Status) ≤ 2
  5. Patients with a life expectancy ≥ 12 weeks as judged by the investigator
  6. At least one measurable lesion or evaluable lesion defined by the Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1
* Lung Cancer

  1. Male or female at least 18 years old or older at the time of informed consent
  2. Histologically or cytologically confirmed carcinoma of the lung (small cell lung cancer not included)
  3. Patients who have unresectable metastatic lesion
  4. ECOG PS (Eastern Cooperative Oncology Group Performance status) ≤ 2
  5. Patients with a life expectancy ≥ 12 weeks as judged by the investigator
  6. At least one measurable lesion or evaluable lesion defined by the Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1

Exclusion Criteria:

* Breast Cancer

  1. History of malignancy other than metastatic triple negative breast cancer within 5 years prior to the first dose of investigational product (however, patients with effectively treated skin cancer, thyroid cancer, and carcinoma in situ that has been in complete remission for at least 3 years and thus considered cured by the investigator are eligible)
  2. Uncontrolled CNS metastasis (however, patients with treated and stable brain metastasis (radiographically stable for at least 30 days without steroids) are eligible)
  3. Primary cancer-related complications potentially requiring urgent surgery as judged by the investigator
  4. Grade ≥ 3 active infection requiring intravenous antibiotics per NCI-CTCAE version 5.0
  5. History of one or more of the following cardiovascular diseases

     * Cerebrovascular disease, unstable angina, or myocardial infarction within 6 months prior to the screening visit (Visit 1)
     * Congestive heart failure corresponding to New York Heart Association (NYHA) Class III or above (see Appendix 1. NYHA Classification)
     * Serious cardiac arrhythmia not controlled with medication or clinically significant cardiovascular abnormality as judged by the investigator
     * QTc \> 480 msec (Fredericia's formula) during 12-lead ECG at screening visit (Visit 1)
  6. Pregnant women, breast-feeding women or women with a positive pregnancy test at screening visit (Visit 1)
  7. Renal impairment or chronic renal failure patient requiring hemo- or peritoneal dialysis
  8. Previous treatment with the investigational product
  9. Treatment with other investigational product within 30 days prior to the first dose of the investigational product
  10. Unable to come to the site hospital on a daily basis for investigational product administration
  11. Patients who are otherwise considered to be ineligible for this study based on investigator's judgment.
* Pancreatic Cancer

  1. History of malignancy other than advanced or metastatic pancreatic adenocarcinoma within 5 years prior to the first dose of investigational product (however, patients with effectively treated skin cancer, thyroid cancer, and carcinoma in situ that has been in complete remission for at least 3 years and thus considered cured by the investigator are eligible)
  2. Uncontrolled CNS metastasis (however, patients with treated and stable brain metastasis (radiographically stable for at least 30 days without steroids) are eligible)
  3. Primary cancer-related complication potentially requiring urgent surgery as judged by the investigator
  4. Grade ≥ 3 active infection requiring intravenous antibiotics per NCI-CTCAE version 5.0
  5. History of one or more of the following cardiovascular diseases

     * Cerebrovascular disease, unstable angina, or myocardial infarction within 6 months prior to the screening visit (Visit 1)
     * Congestive heart failure corresponding to New York Heart Association (NYHA) Class III or above (see Appendix 1. NYHA Classification)
     * Serious cardiac arrhythmia not controlled with medication or clinically significant cardiovascular abnormality as judged by the investigator
     * QTc \> 480 msec (Fredericia's formula) during 12-lead ECG at screening visit (Visit 1)
  6. Pregnant women, breast-feeding women or women with a positive pregnancy test at screening visit (Visit 1)
  7. Renal impairment or chronic renal failure patient requiring hemo- or peritoneal dialysis
  8. Previous treatment with the investigational product
  9. Treatment with other investigational product within 30 days prior to the first dose of the investigational product
  10. Unable to come to the site hospital on a daily basis for investigational product administration
  11. Patients who are otherwise considered to be ineligible for this study based on investigator's judgment
* Lung Cancer

  1. History of malignancy other than metastatic non-small cell lung cancer within 5 years prior to the first dose of investigational product (however, patients with effectively treated skin cancer, thyroid cancer, and carcinoma in situ that has been in complete remission for at least 3 years and thus considered cured by the investigator are eligible)
  2. Uncontrolled CNS metastasis (however, patients with treated and stable brain metastasis (radiographically stable for at least 30 days) are eligible)
  3. Primary cancer-related complication potentially requiring urgent surgery as judged by the investigator
  4. Grade ≥ 3 active infection requiring intravenous antibiotics per NCI-CTCAE version 5.0
  5. History of one or more of the following cardiovascular diseases

     * Cerebrovascular disease, unstable angina, or myocardial infarction within 6 months prior to the screening visit (Visit 1)
     * Congestive heart failure corresponding to New York Heart Association (NYHA) Class III or above (see Appendix 1. NYHA Classification)
     * Serious cardiac arrhythmia not controlled with medication or clinically significant cardiovascular abnormality as judged by the investigator
     * QTc \> 480 msec (Fredericia's formula) during 12-lead ECG at screening visit (Visit 1)
  6. Pregnant women, breast-feeding women or women with a positive pregnancy test at screening visit (Visit 1)
  7. Renal impairment or chronic renal failure patient requiring hemo- or peritoneal dialysis
  8. Previous treatment with the investigational product
  9. Treatment with other investigational product within 30 days prior to the first dose of the investigational product
  10. Unable to come to the site hospital on a daily basis for investigational product administration
  11. Patients who are otherwise considered to be ineligible for this study based on investigator's judgment