We're building a better ClinicalTrials.gov. Check it out and tell us what you think!
Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu

Study of TRC105 With Abiraterone and With Enzalutamide in Prostate Cancer Patients Progressing on Therapy

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03418324
Recruitment Status : Completed
First Posted : February 1, 2018
Results First Posted : December 30, 2020
Last Update Posted : December 30, 2020
Sponsor:
Information provided by (Responsible Party):
Edwin Posadas, MD, Cedars-Sinai Medical Center

Brief Summary:
This research study is being done to measure the clinical benefit of TRC105 in combination with abiraterone or enzalutamide in metastatic, castration-resistant prostate cancer patients who are taking either abiraterone or enzalutamide and showing signs of biochemical progression without radiographic progression. A patient who is progressing on AR-therapy will continue the same AR-therapy on study with the addition of TRC105. The two arms will accrue in parallel and independently.

Condition or disease Intervention/treatment Phase
Prostate Cancer Drug: TRC105 Drug: Abiraterone Drug: Enzalutamide Phase 2

Detailed Description:

This is a Phase II, open-label study of TRC105 (anti-endoglin antibody) in combination with abiraterone or enzalutamide in metastatic, castration-resistant prostate cancer patients who are taking either abiraterone or enzalutamide and showing signs of biochemical progression without radiographic progression. A patient who is progressing on AR-therapy will continue the same AR-therapy on study with the addition of TRC105. The two arms will accrue in parallel and independently.

There will be a 2-week washout of the active AR-targeted therapy prior to initiation of combination therapy. Tumor response should be assessed at a frequency of 8 weeks by CT/MRI chest, abdomen and pelvis as well as bone scan. Patients may continue on therapy until radiographic progression by RECIST 1.1 or PCWG3 criteria.

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 11 participants
Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Intervention Model Description: Bayesian design
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Phase 2 Study of TRC105 (Anti-endoglin Antibody) With Abiraterone and With Enzalutamide in Metastatic, Castration Resistant Prostate Cancer Patients Progressing on Therapy
Actual Study Start Date : March 5, 2018
Actual Primary Completion Date : November 6, 2019
Actual Study Completion Date : November 6, 2019

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Prostate Cancer

Arm Intervention/treatment
Experimental: Arm A: TRC105 + Abiraterone
Patients progressing on Abiraterone will undergo a washout period and then continue treatment with TRC105 + Abiraterone
Drug: TRC105
Patients will receive TRC105 10mg weekly x 4, and then 15 mg/kg every 2 weeks
Other Name: Carotuximab

Drug: Abiraterone
Patients who are progressing on Abiraterone will undergo a washout period and then continue treatment with standard dosing of Abiraterone plus TRC105.
Other Name: Zytiga

Experimental: Arm E: TRC105 + Enzalutamide
Patients progressing on Enzalutamide will undergo a washout period and then continue treatment with TRC105 + Enzalutamide
Drug: TRC105
Patients will receive TRC105 10mg weekly x 4, and then 15 mg/kg every 2 weeks
Other Name: Carotuximab

Drug: Enzalutamide
Patients who are progressing on Enzalutamide will undergo a washout period and then continue standard treatment with Enzalutamide plus TRC105.
Other Name: Xtandi




Primary Outcome Measures :
  1. Overall Clinical Benefit [ Time Frame: Through study completion, average 24 months ]

    Number of participants with stabilization of disease for at least 2 months or disease improvement at any time from start of combination therapy by radiographic and/or biochemical criteria through treatment completion up to an estimated period of 24 months

    • radiographic improvement defined as a PR (At least a 30% decrease in the sum of the diameters of target lesions, taking as reference the baseline sum. There can be no appearance of new lesions) or CR (Disappearance of all target lesions, determined by two separate observations conducted not less than 4 weeks apart. There can be no appearance of new lesions) by RECIST 1.1 or improvement by PCWG3 criteria
    • Biochemical response will be defined by PCWG3 criteria
    • Stabilization will be defined as the absence of progression by BOTH radiographic and biochemical criteria


Secondary Outcome Measures :
  1. Adverse Events From TRC105 and Abiraterone or Enzalutamide [ Time Frame: 4 months ]
    Number of participants with grade 3/4 Adverse Events Related to investigational therapy as assessed Using CTCAE (v.4) up to 4 months from treatment initiation.

  2. Progression Free Survival [ Time Frame: 24 months ]

    Time (in Months) from treatment initiation to radiographic and clinical progression over study duration (estimated 24 months)

    - radiographic criteria measured by RECIST 1.1 [Progressive Disease (PD): At least a 20% increase in the sum of the diameters of target lesions plus an absolute increase of at least 5 mm, taking as reference the smallest sum recorded since the start of study]


  3. Clinical Benefit at Two Months [ Time Frame: 2 months ]

    Proportion of participants with stabilization of disease for two months or disease improvement at anytime from start of combination therapy to two months by radiographic and/or biochemical criteria

    • radiographic improvement defined as a PR (At least a 30% decrease in the sum of the diameters of target lesions, taking as reference the baseline sum. There can be no appearance of new lesions) or CR (Disappearance of all target lesions, determined by two separate observations conducted not less than 4 weeks apart. There can be no appearance of new lesions) by RECIST 1.1 or improvement by PCWG3 criteria
    • Biochemical response will be defined by PCWG3 criteria
    • Stabilization will be defined as the absence of progression by BOTH radiographic and biochemical criteria

  4. Clinical Benefit at Four Months [ Time Frame: 4 months ]

    Proportion of participants with stabilization of disease for at least 4 months or disease improvement at anytime from start of combination therapy to four months by radiographic and/or biochemical criteria

    • radiographic improvement defined as a PR (At least a 30% decrease in the sum of the diameters of target lesions, taking as reference the baseline sum. There can be no appearance of new lesions) or CR (Disappearance of all target lesions, determined by two separate observations conducted not less than 4 weeks apart. There can be no appearance of new lesions) by RECIST 1.1 or improvement by PCWG3 criteria
    • Biochemical response will be defined by PCWG3 criteria
    • Stabilization will be defined as the absence of progression by BOTH radiographic and biochemical criteria

  5. Clinical Benefit From PSA Serum Concentration (2 Months) [ Time Frame: 2 months ]
    Proportion of participants with stabilization of disease based on PSA serum concentration levels. Stabilization of disease refers to PSA values that do not meet criteria for progression where progression will be defined as a rise in serum PSA that is ≥ 25% and 2 ng/mL above nadir which is confirmed by a second value ≥ 3 weeks later.

  6. Clinical Benefit From PSA Serum Concentration (4 Months) [ Time Frame: 4 months ]
    Proportion of participants with stabilization of disease based on PSA serum concentration levels. Stabilization of disease refers to PSA values that do not meet criteria for progression where progression will be defined as a rise in serum PSA that is ≥ 25% and 2 ng/mL above nadir which is confirmed by a second value ≥ 3 weeks later.



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   Male
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. History of metastatic, castration-resistant prostate cancer with rising PSA on either abiraterone or enzalutamide

    • PSA rise will be defined as an increase in PSA of 0.2 ng/mL or higher on at least 2 separate occasions greater than 1 week apart while on either abiraterone or enzalutamide
    • If there is a drop in serum PSA after the first rise, and the patient has another PSA rise which is greater than the first, the patient will still be considered eligible.
  2. ECOG 0-2
  3. Resolution of adverse events results as described below.

    • Laboratory abnormalities must meet values specified below in criteria #4
    • If the patient's most recent line of therapy is treatment with abiraterone or enzalutamide, then all adverse events must be resolved to Grade 2 or better
    • If the most recent line of therapy is any other treatment for mCRPC then all Adverse events must be resolved to grade 1 or better, with the exception of fatigue, alopecia and neuropathy (which must resolve to CTCAE grade 2)
  4. Adequate organ function defined by:

    • AST and ALT < 2.5 x ULN
    • Total serum bilirubin < 1.5 x ULN
    • Platelets > 60,000
    • Hgb > 8.5 g/dL
    • Serum Cr <1.5 x ULN or a creatinine clearance > 30.
    • INR ≤ 1.2 unless the patient is receiving a direct Factor Xa inhibitor or a direct thrombin inhibitor
  5. Patients must be surgically sterile or must agree to use effective contraception during the study and for 3 months following last dose of TRC105. The definition of effective contraception will be based on the judgment of the Principal Investigator or a designated associate. Abstinence from intercourse is an acceptable form of contraception.

Exclusion Criteria:

  1. Non-PSA producing prostate cancers- such as small cell prostate cancers or those prostate cancers which exhibit radiographic progression without PSA rise
  2. Inability to tolerate standard doses of abiraterone (1000 mg daily) or enzalutamide (160 mg daily).
  3. Other prior malignancy requiring active anticancer therapy
  4. Prior exposure to TRC105 or any CD105 targeted antibody
  5. Any major surgical procedure within 2 weeks of starting therapy
  6. Uncontrolled chronic hypertension defined as sustained by systolic pressure (SBP) >150 mmHg or diastolic pressure (DBP) >90 despite optimal therapy.
  7. Active bleeding or pathologic conditions that carries a high bleeding risk
  8. Use of thrombolytics within 10 days prior to the first day of TRC105
  9. Known hypersensitivity to Chinese hamster ovary products or other recombinant human, chimeric, or humanized antibodies
  10. A known diagnosis of Osler-Weber-Rendu syndrome
  11. Ascites or pericardial or pleural effusion requiring external drainage procedures
  12. History of untreated brain involvement with cancer, spinal cord compression, or carcinomatous meningitis, or new evidence of brain or leptomeningeal disease. Patients with radiated or resected lesions are permitted, provided the lesions are fully treated and inactive, patients are asymptomatic, and no steroids have been administered for at least 28 days. Imaging for CNS disease will not be required for screening unless there is a history of a neurological finding such as new onset weakness or numbness that cannot be explained by other medical history.
  13. Acute cardiovascular event within the past 6 months. An acute cardiovascular event will be defined as a myocardial infraction, NYHA Class II or worse congestive heart failure, cerebrovascular accident, transient ischemic attack, arterial embolism, pulmonary embolism, percutaneous transluminal coronary angioplasty (PTCA), or CABG. Deep venous thrombosis within 6 months, unless the patient is anti-coagulated without the use of warfarin for at least 2 weeks. In this situation, low molecular weight heparin is preferred.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03418324


Locations
Layout table for location information
United States, California
Cedars Sinai Medical Center
Los Angeles, California, United States, 90048
Sponsors and Collaborators
Cedars-Sinai Medical Center
Investigators
Layout table for investigator information
Principal Investigator: Edwin Posadas, MD FACP Cedars-Sinai Medical Center Samuel Oschin Comprehensive Cancer Institute
  Study Documents (Full-Text)

Documents provided by Edwin Posadas, MD, Cedars-Sinai Medical Center:
Layout table for additonal information
Responsible Party: Edwin Posadas, MD, Medical Director, Urologic Oncology Program, Cedars-Sinai Medical Center
ClinicalTrials.gov Identifier: NCT03418324    
Other Study ID Numbers: IIT2016-16-POSADAS-TRC105
First Posted: February 1, 2018    Key Record Dates
Results First Posted: December 30, 2020
Last Update Posted: December 30, 2020
Last Verified: December 2020

Layout table for additional information
Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Edwin Posadas, MD, Cedars-Sinai Medical Center:
Prostate Cancer
Metastatic Prostate Cancer
Castration Resistant Prostate Cancer
Metastatic Castration Resistant
Additional relevant MeSH terms:
Layout table for MeSH terms
Prostatic Neoplasms
Genital Neoplasms, Male
Urogenital Neoplasms
Neoplasms by Site
Neoplasms
Prostatic Diseases