Phase I TH-302 Plus Gemcitabine Plus Nab-Paclitaxel in Pancreatic Cancer
Status: | Terminated |
---|---|
Conditions: | Cancer, Cancer, Pancreatic Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 12/17/2017 |
Start Date: | January 2014 |
End Date: | May 2016 |
An Open-Label, Phase I Dose Escalation Trial of TH-302 in Combination With Gemcitabine and Nab-Paclitaxel in Previously Untreated Subjects With Metastatic or Locally Advanced Unresectable Pancreatic Adenocarcinoma
This is a multicenter, open-label, Phase 1, dose escalation trial to evaluate the safety,
tolerability, and recommended Phase 2 dose (RP2D) of TH-302 in combination with gemcitabine
and nab-paclitaxel in previously untreated subjects with locally advanced unresectable or
metastatic pancreatic adenocarcinoma.
tolerability, and recommended Phase 2 dose (RP2D) of TH-302 in combination with gemcitabine
and nab-paclitaxel in previously untreated subjects with locally advanced unresectable or
metastatic pancreatic adenocarcinoma.
Inclusion Criteria:
- Subjects greater than or equal to (>=) 18 years of age with locally advanced
unresectable or metastatic pancreatic adenocarcinoma proven by histology or cytology
and previously untreated with chemotherapy or systemic therapy other than:
- Radiosensitizing doses of 5-fluorouracil;
- Radiosensitizing doses of gemcitabine if relapse occurred at least 6 months after
completion of gemcitabine;
- Neoadjuvant chemotherapy if relapse occurred at least 6 months after surgical
resection;
- Adjuvant chemotherapy if relapse occurred at least 6 months after completion of
adjuvant chemotherapy
- Subjects may have measurable or non-measurable disease according to RECIST 1.1.
- Eastern cooperative oncology group (ECOG) performance status of 0 or 1
- Acceptable hematological status, liver and renal function as defined in the protocol
- Other protocol defined inclusion criteria could apply
Exclusion Criteria:
- Significant cardiac or peripheral vascular arterial disease
- Known brain, leptomeningeal or epidural metastases (unless treated and well controlled
for at least 3 months)
- Severe chronic obstructive or other pulmonary disease with hypoxemia
- Active, uncontrolled bacterial, viral, or fungal infections, requiring systemic
therapy
- Subjects receiving concomitant treatment with radiotherapy or other investigational
drugs
- Other protocol defined exclusion criteria could apply
We found this trial at
5
sites
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Dana-Farber Cancer Institute Since it’s founding in 1947, Dana-Farber has been committed to providing adults...
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