Kidney CancerPhase 1NCT01497444
Sorafenib Tosylate and Hypoxia-Activated Prodrug TH-302 in Treating Patients With Advanced Kidney Cancer or Liver Cancer That Cannot Be Removed By Surgery
A Phase 1 study testing hypoxia-activated prodrug TH-302 and sorafenib tosylate in people with Kidney Cancer and Liver Cancer, run by Alliance for Clinical Trials in Oncology at 2 sites in United States.
Trial summary
RATIONALE: Sorafenib tosylate may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth by blocking blood flow to the tumor. Drugs used in chemotherapy, such as hypoxia-activated prodrug TH-302, work in different ways to stop the growth of tumor cells, either by killing the cells or by… Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Kidney Cancer, Liver Cancer
- What is being tested?
- hypoxia-activated prodrug TH-302 and sorafenib tosylate
- Type of treatment
- Pill or oral medicine, Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 24 participants
- Where
- 2 sitesUnited States
- Study dates
- May 2012to 1 Nov 2019
- Phase
- Phase 1
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Phase I Registration - Inclusion Criteria
- Age ≥18 years
- Cytological or histological confirmed diagnosis of advanced hepatocellular or renal cell carcinoma. HCC patients should not be amenable to treatment with surgery or to orthotopic liver transplant.
- Patients must have measurable disease as defined in the protocol.
- RCC patients only: Tumor progression after receiving standard/approved chemotherapy and/or targeted agent, where there is no approved therapy or for tumors where sorafenib based therapy would be standard therapy.
- HCC patients only:
- First line (i.e., no prior systemic therapy) or second line (with prior first line sorafenib therapy only) advanced HCC.
- Child Pugh class A or B7 liver disease
- Prior chemoembolization, radioembolization, radiofrequency ablation (RFA), or other local ablative therapies are permissible if ≥6 weeks from procedure with evidence of progression or new metastatic disease, if applicable.
- ECOG Performance Status (PS) 0 or 1.
- The following laboratory values obtained ≤14 days prior to registration.
- Absolute neutrophil count (ANC) ≥1200/mm3
- Peripheral Platelet Count (PLT) ≥75,000/mm3
- Hemoglobin (HgB) >8.5 g/dL
- Bilirubin ≤3.0 x upper limit of normal (ULN)
- SGOT (AST) ≤2.5 x ULN, if subject has HCC or liver metastases ≤5 x UL
- SGPT (ALT) ≤2.5 x ULN, if subject has HCC or liver metastases ≤5 x ULN
- Creatinine ≤1.5 x ULN
- INR ≤1.5 x ULN. Patients receiving anti-coagulation therapy are permitted as long as they have a stable INR≤3.0.
- Negative pregnancy test done ≤7 days prior to registration, for women of childbearing potential only.
- Provide informed written consent.
- Willing to return to Alliance enrolling institution for follow-up.
- Life expectancy ≥3 months.
Phase I Registration - Exclusion Criteria
- Any of the following because this study involves an investigational agent whose genotoxic, mutagenic and teratogenic effects on the developing fetus and newborn are unknown.
- Pregnant women
- Nursing women
- Men or women of childbearing potential who are unwilling to employ adequate contraception for the duration of study participation. Men and women should continue to use adequate birth control after the last administration of sorafenib and TH-302 under the guidance of their treating physician.
- Co-morbid systemic illnesses or other severe concurrent disease which, in the judgment of the investigator, would make the patient inappropriate for entry into this study or interfere significantly with the proper assessment of safety and toxicity of the prescribed regimens.
- Receiving any other investigational agent.
- Other active malignancy ≤3 years prior to registration. EXCEPTIONS: Non-melanotic skin cancer or carcinoma-in-situ of the cervix. NOTE: If there is a history or prior malignancy, they must not be receiving other specific treatment (other than hormonal therapy) for their cancer.
- Inadequately controlled hypertension (systolic blood pressure of >150 mmHg or diastolic pressure >100 mmHg on anti-hypertensive medications).
- Major surgical procedures, or significant traumatic injury ≤14 days prior to registration or anticipation of need for elective or planned major surgical procedure during the course of the study.
- New York Heart Association (NYHA) classification III or IV congestive heart failure.
- Received treatment with radiation therapy or investigational therapy ≤28 days prior to registration.
- RCC patients only: Having received chemotherapy prior to study entry within 5 half-lives of the agent (as described in the package insert), or 4 weeks prior to registration (whichever is shorter) with resolution of side effects from therapy to ≤grade 1.
- Known central nervous system or brain metastasis that are either symptomatic or untreated. Note: Patients with neurological symptoms must undergo a CT scan/MRI of the brain to exclude brain metastasis.
- Note: Subjects with CNS metastases that have been treated and are stable without symptoms for ≥ 4 weeks after completion of treatment are eligible.
- HCC patients only: Cancer potentially amenable to local modalities of therapy or surgical resection.
- Known or suspected allergy or hypersensitivity to any component of TH-302, sorafenib, or any of the sorafenib excipients.
- Any condition that severely impairs patient's ability to swallow whole pills.
- QTc interval >500 msec on baseline EKG.
- Documented history of prolonged QTc interval ≤ 6 months prior to registration.
- Receiving any medication that has documented data or is generally accepted as having increased risk of QT prolongation and/or Torsades de Pointes.
- Receiving any medications or substances that are inducers or strong or moderate inhibitors of CYP3A4, see the protocol for a complete listing.
- Fibrolamellar histology HCC, mixed hepatocholangiocarcinoma, hepatic sarcomas and other non-HCC primary liver tumors.
- History of lobectomy involving >50% of lobe.
- Radioembolization within 8 weeks of Day 1 dosing of sorafenib.
Phase II Registration - Inclusion Criteria
- Age ≥18 years
- Cytological or histological confirmed diagnosis of hepatocellular carcinoma that is locally advanced or metastatic and is not amenable to treatment with surgery or to orthotopic liver transplant.
- Patients must have measurable disease as defined in Section 11.0 must have at least one non-nodal lesion.
- First line advanced HCC (i.e., no prior systemic therapy).
- Child Pugh class A or B7 liver disease
- Prior chemoembolization, radioembolization, radiofrequency ablation (RFA), or other local ablative therapies are permissible if ≥6 weeks from procedure with evidence of progression or new metastatic disease, if applicable.
- ECOG Performance Status (PS) 0 or 1.
- The following laboratory values obtained ≤14 days prior to registration.
- Absolute neutrophil count (ANC) ≥1200/mm^3
- Peripheral Platelet Count (PLT) ≥75,000/mm^3
- Hemoglobin (HgB) >8.5 g/dL
- Total bilirubin ≤3.0 x upper limit of normal (ULN)
- SGOT (AST) ≤5 x ULN.
- SGPT (ALT) ≤5 x ULN.
- Creatinine ≤1.5 x ULN.
- INR ≤1.5 x ULN. Patients receiving anti-coagulation therapy are permitted as long as they have a stable INR≤3.0.
- Negative pregnancy test done ≤7 days prior to registration, for women of childbearing potential only.
- Provide informed written consent.
- Willing to return to Alliance enrolling institution for follow-up.
- Life expectancy ≥3 months.
- Ability to receive intravenous contrast for the purpose of imaging.
Phase II Registration - Exclusion Criteria
- Any of the following because this study involves an investigational agent whose genotoxic, mutagenic and teratogenic effects on the developing fetus and newborn are unknown.
- Pregnant women
- Nursing women
- Men or women of childbearing potential who are unwilling to employ adequate contraception for the duration of study participation. Men and women should continue to use adequate birth control after the last administration of sorafenib and TH-302 under the guidance of their treating physician.
- Co-morbid systemic illnesses or other severe concurrent disease which, in the judgment of the investigator, would make the patient inappropriate for entry into this study or interfere significantly with the proper assessment of safety and toxicity of the prescribed regimens.
- Receiving any other investigational agent.
- Other active malignancy ≤3 years prior to registration. EXCEPTIONS: Non-melanotic skin cancer or carcinoma-in-situ of the cervix. NOTE: If there is a history or prior malignancy, they must not be receiving other specific treatment (other than hormonal therapy) for their cancer.
- Inadequately controlled hypertension (systolic blood pressure of >150 mmHg or diastolic pressure >100 mmHg on anti-hypertensive medications).
- Major surgical procedures, or significant traumatic injury ≤14 days prior to registration or anticipation of need for elective or planned major surgical procedure during the course of the study.
- New York Heart Association (NYHA) classification III or IV congestive heart failure.
- Received treatment with radiation therapy or investigational therapy ≤28 days prior to registration.
- Known central nervous system or brain metastasis that are either symptomatic or untreated. Note: Patients with neurological symptoms must undergo a CT scan/MRI of the brain to exclude brain metastasis.
- Note: Subjects with CNS metastases that have been treated and are stable without symptoms for ≥ 4 weeks after completion of treatment are eligible.
- Fibrolamellar histology HCC, mixed hepatocholangiocarcinoma, hepatic sarcomas and other non-HCC primary liver tumors.
- Cancer potentially amenable to local modalities of therapy or surgical resection.
- Known or suspected allergy or hypersensitivity to any component of TH-302, sorafenib, or any of the sorafenib excipients
- Any condition that severely impairs patient's ability to swallow whole pills.
- QTc interval >500 msec on baseline EKG.
- Documented history of prolonged QTc interval ≤ 6 months prior to registration.
- Receiving any medication that has documented data or is generally accepted as having increased risk of QT prolongation and/or Torsades de Pointes.
- Receiving any medications or substances that are inducers or strong or moderate inhibitors of CYP3A4, please see protocol for a complete listing.
- History of lobectomy involving >50% of lobe.
- Radioembolization within 8 weeks of Day 1 dosing of sorafenib.
Trial locations and contacts
2 sites in 1 country.
United States2 sites
Mayo Clinic Cancer Center
Rochester, Minnesota, 55905
Mayo Clinic Scottsdale
Scottsdale, Arizona, 85259-5499
About this study
Official title: Study of Sorafenib + TH-302: Phase I in Advanced Renal Cell Carcinoma (RCC) and Advanced Hepatocellular Carcinoma (HCC) and Phase II in 1st Line Advanced HCC
RATIONALE: Sorafenib tosylate may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth by blocking blood flow to the tumor. Drugs used in chemotherapy, such as hypoxia-activated prodrug TH-302, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving sorafenib tosylate together with hypoxia-activated prodrug TH-302 may kill more tumor cells.
PURPOSE: This phase I/II trial studies the side effects and best dose of giving sorafenib tosylate together with hypoxia-activated prodrug TH-302 and to see how well they work in treating patients with advanced kidney cancer or liver cancer that cannot be removed by surgery.
Read the detailed description
OBJECTIVES:
Primary
- To determine the maximum-tolerated dose (MTD) and recommended Phase II dosing (RP2D) for the combination of sorafenib tosylate and hypoxia-activated prodrug TH-302 (TH-302) in patients with hepatocellular carcinoma (HCC) and renal cell carcinoma (RCC; non-HCC) advanced solid tumors. (Phase I)
- To evaluate the overall response rate (RR) determined based on modified RECIST criteria (Lencioni and Llovet 2010) in patients with advanced HCC receiving sorafenib tosylate with TH-302. (Phase II)
Secondary
- To characterize overall toxicity profile of sorafenib tosylate + TH-302 within patients with HCC and RCC (non-HCC) advanced solid tumors. (Phase I)
- To characterize the responses of sorafenib tosylate + TH-302 within patients with HCC and RCC (non-HCC) advanced solid tumors. (Phase I)
- To assess the adverse events (AEs) profile and safety profile of sorafenib tosylate in combination with TH-302 in patients with advanced HCC. (Phase II)
- To estimate the overall response rate based on standard RECIST criteria in the study population. (Phase II)
- To estimate the duration of response based on modified (standard) RECIST criteria in the study population. (Phase II)
- To estimate the progression free survival (PFS) in the study population. (Phase II)
- To estimate the overall survival (OS) in the study population. (Phase II)
- To estimate the alpha-fetoprotein (AFP) response rate (defined as > 20% decrease of AFP from baseline) in the study population. (Phase II)
OUTLINE: This is a multicenter, phase I dose-escalation study followed by a phase II study.
Patients receive sorafenib tosylate orally (PO) twice daily (BID) on days 1-28 and hypoxia-activated prodrug TH-302 IV over 30 minutes on days 8, 15, and 22. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.
Some patients undergo blood sample collection periodically during study for alpha-fetoprotein analysis.
After completion of study treatment, patients are followed up for 3 years.
- Conditions
- Kidney Cancer, Liver Cancer
- Being tested
- hypoxia-activated prodrug TH-302, sorafenib tosylate
- Keywords
- recurrent adult primary liver cancer, recurrent renal cell cancer, advanced adult primary liver cancer, localized unresectable adult primary liver cancer, adult primary hepatocellular carcinoma
- Medical subject headings
- Kidney Neoplasms, Liver Neoplasms, Carcinoma, Hepatocellular, Carcinoma, Renal Cell
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
hypoxia-activated prodrug TH-302Drug
sorafenib tosylateDrug
| Study group | Role | What they receive |
|---|---|---|
| sorafenib and TH-302 | Experimental | Patients will be administered sorafenib tablets to take twice daily by mouth, every day of each cycle. Patients will also be given TH-302 intravenously (IV) on days 8, 15 and 22 of each cycle. A cycle is 28 days. Receives: Drug: hypoxia-activated prodrug TH-302; Drug: sorafenib tosylate |
What is being measured
The primary outcome is the main question the study is designed to answer.
Number of dose-limiting toxicity incidents as assessed by CTCAE version 4.0 (Phase I)
Measured: Up to 24 weeks
MTD of sorafenib tosylate and TH-302 (Phase I)
Measured: Up to 24 weeks
Overall response rate (Phase II)
Measured: Up to 3 years
Secondary outcomes (6)
Adverse events as assessed by NCI CTCAE version 4.0 (Phase II)
Measured: Up to 3 years
Overall response rate based on standard RECIST criteria (Phase II)
Measured: Up to 3 years
Duration of response based on modified (standard) RECIST criteria (Phase II)
Measured: Up to 3 years
PFS (Phase II)
Measured: Up to 3 years
OS (Phase II)
Measured: Up to 3 years
AFP response rate (Phase II)
Measured: Up to 3 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted22 Dec 2011 (estimated)
- Study startMay 2012
- Primary completionJan 2016
- Study completion1 Nov 2019
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Kidney CancerStudies of the same condition, open and under way.
- More trials run by Alliance for Clinical Trials in OncologyThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 1
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 24 participants (actual)
Sponsor and investigators
- Lead sponsor
- Alliance for Clinical Trials in Oncology
- Sponsor type
- University, hospital or other
- Collaborators
- National Cancer Institute (NCI), Threshold Pharmaceuticals
- Responsible party
- Sponsor
- Investigators
- Mitesh J. Borad, MD, Study chair, Mayo Clinic
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01497444
- Sponsor's protocol ID
- N1153
- Other IDs
- NCCTG-N1153, CDR0000720022, NCI-2012-00095, U10CA031946
- Status last verified
- Feb 2020
- First submitted
- 20 Dec 2011
- Last updated
- 6 Feb 2020
- Results posted
- No
- Data monitoring committee
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 6 Feb 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Study of Sorafenib + TH-302: Phase I in Advanced Renal Cell Carcinoma (RCC) and Advanced Hepatocellular Carcinoma (HCC) and Phase II in 1st Line Advanced HCC
- ClinicalTrials.gov ID
- NCT01497444
- Acronym / sponsor ID
- N1153
- Conditions
- Kidney Cancer, Liver Cancer
- Keywords
- recurrent adult primary liver cancer, recurrent renal cell cancer, advanced adult primary liver cancer, localized unresectable adult primary liver cancer, adult primary hepatocellular carcinoma
- Phase
- Phase 1
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 24 participants (actual)
- Lead sponsor
- Alliance for Clinical Trials in OncologyUniversity, hospital or other
- Collaborators
- National Cancer Institute (NCI), Threshold Pharmaceuticals
- Study start
- May 2012 (actual)
- Primary completion
- Jan 2016 (actual)
- Study completion
- 1 Nov 2019 (actual)
- First posted
- 22 Dec 2011 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
RATIONALE: Sorafenib tosylate may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth by blocking blood flow to the tumor. Drugs used in chemotherapy, such as hypoxia-activated prodrug TH-302, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving sorafenib tosylate together with hypoxia-activated prodrug TH-302 may kill more tumor cells.
PURPOSE: This phase I/II trial studies the side effects and best dose of giving sorafenib tosylate together with hypoxia-activated prodrug TH-302 and to see how well they work in treating patients with advanced kidney cancer or liver cancer that cannot be removed by surgery.
Detailed description
OBJECTIVES:
Primary
- To determine the maximum-tolerated dose (MTD) and recommended Phase II dosing (RP2D) for the combination of sorafenib tosylate and hypoxia-activated prodrug TH-302 (TH-302) in patients with hepatocellular carcinoma (HCC) and renal cell carcinoma (RCC; non-HCC) advanced solid tumors. (Phase I)
- To evaluate the overall response rate (RR) determined based on modified RECIST criteria (Lencioni and Llovet 2010) in patients with advanced HCC receiving sorafenib tosylate with TH-302. (Phase II)
Secondary
- To characterize overall toxicity profile of sorafenib tosylate + TH-302 within patients with HCC and RCC (non-HCC) advanced solid tumors. (Phase I)
- To characterize the responses of sorafenib tosylate + TH-302 within patients with HCC and RCC (non-HCC) advanced solid tumors. (Phase I)
- To assess the adverse events (AEs) profile and safety profile of sorafenib tosylate in combination with TH-302 in patients with advanced HCC. (Phase II)
- To estimate the overall response rate based on standard RECIST criteria in the study population. (Phase II)
- To estimate the duration of response based on modified (standard) RECIST criteria in the study population. (Phase II)
- To estimate the progression free survival (PFS) in the study population. (Phase II)
- To estimate the overall survival (OS) in the study population. (Phase II)
- To estimate the alpha-fetoprotein (AFP) response rate (defined as > 20% decrease of AFP from baseline) in the study population. (Phase II)
OUTLINE: This is a multicenter, phase I dose-escalation study followed by a phase II study.
Patients receive sorafenib tosylate orally (PO) twice daily (BID) on days 1-28 and hypoxia-activated prodrug TH-302 IV over 30 minutes on days 8, 15, and 22. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.
Some patients undergo blood sample collection periodically during study for alpha-fetoprotein analysis.
After completion of study treatment, patients are followed up for 3 years.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| sorafenib and TH-302 | Experimental | Drug: hypoxia-activated prodrug TH-302, Drug: sorafenib tosylatePatients will be administered sorafenib tablets to take twice daily by mouth, every day of each cycle. Patients will also be given TH-302 intravenously (IV) on days 8, 15 and 22 of each cycle. A cycle is 28 days. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| hypoxia-activated prodrug TH-302 | Drug | sorafenib and TH-302 |
| sorafenib tosylate | Drug | sorafenib and TH-302 |
Primary outcome
Number of dose-limiting toxicity incidents as assessed by CTCAE version 4.0 (Phase I)
Time frame: Up to 24 weeks
MTD of sorafenib tosylate and TH-302 (Phase I)
Time frame: Up to 24 weeks
Overall response rate (Phase II)
Time frame: Up to 3 years
6 secondary outcomes
Adverse events as assessed by NCI CTCAE version 4.0 (Phase II)
Time frame: Up to 3 years
Overall response rate based on standard RECIST criteria (Phase II)
Time frame: Up to 3 years
Duration of response based on modified (standard) RECIST criteria (Phase II)
Time frame: Up to 3 years
PFS (Phase II)
Time frame: Up to 3 years
OS (Phase II)
Time frame: Up to 3 years
AFP response rate (Phase II)
Time frame: Up to 3 years
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 6 Feb 2020.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Mitesh J. Borad, MD study chair
Mayo Clinic
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 1 study testing hypoxia-activated prodrug TH-302 and sorafenib tosylate in people with Kidney Cancer and Liver Cancer, run by Alliance for Clinical Trials in Oncology at 2 sites in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 6 Feb 2020. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Number of dose-limiting toxicity incidents as assessed by CTCAE version 4.0 (Phase I) (time frame: Up to 24 weeks). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Feb 2020.