A Study of LOR-253 HCl in Patients With Advanced or Metastatic Solid Tumours
Status: | Completed |
---|---|
Conditions: | Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 3/1/2014 |
Start Date: | January 2011 |
End Date: | June 2013 |
Contact: | Shawn Zhou |
Email: | szhou@lorusthera.com |
Open-Label, Phase 1 Study of LOR-253 HCl in Patients With Advanced or Metastatic Solid Tumours
This is an open-label, phase 1 study to determine the maximum tolerated dose (MTD) or
appropriate target dose if MTD not reached to identify the recommended phase 2 dose of
LOR-253 HCl in patients with advanced or metastatic solid tumours.
appropriate target dose if MTD not reached to identify the recommended phase 2 dose of
LOR-253 HCl in patients with advanced or metastatic solid tumours.
Inclusion Criteria:
1. Male or female 18 years of age or older.
2. Histologically confirmed diagnosis of solid tumour for which no effective therapy is
available or that is unresponsive to conventional therapy.
3. Meet laboratory parameter requirements at study entry.
Exclusion Criteria:
1. Chemotherapy, radiotherapy, biologic therapy, immunotherapy or any other
investigational drugs within 21 days of beginning study treatment with LOR-253 HCl.
2. A hematologic malignancy.
3. A history of brain or other central nervous system metastases.
4. Have a presence of a significant infection.
5. Clinically significant autoimmune disease.
6. Uncontrolled intercurrent illness.
7. With iron or copper overload syndromes.
8. Pregnancy or breast feeding.
We found this trial at
2
sites
1515 Holcombe Blvd
Houston, Texas 77030
Houston, Texas 77030
713-792-2121

University of Texas M.D. Anderson Cancer Center The mission of The University of Texas MD...
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Memorial Sloan-Kettering Cancer Center Memorial Sloan-Kettering Cancer Center — the world's oldest and largest private...
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