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TerminatedNCT04458311ACTIonUpdated Apr 25, 2024

Abiraterone Acetate in Combination With Tildrakizumab

A Phase 1/2 interventional study of Abiraterone Acetate and Tildrakizumab in Metastatic Castration Resistant Prostate Cancer, sponsored by Institute of Cancer Research, United Kingdom. Terminated at 6 sites in 2 countries. Open to male participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-04-25.

Sponsored by Institute of Cancer Research, United Kingdom · Phase 1/2, Interventional, and Health services research

Why this study was terminated
Funder decided that response outcomes to date did not support continuation of the study.

From the registry’s dates

  • Primary completion was Apr 2023, 3 years 6 months ago, and no results have been posted to the registry.
Phase
Phase 1/2
Study type
Interventional
Enrollment
13
Allocation
Non-randomized
Ages
18 Years and older
Sex
Male
01

Study summary

The purpose of this study is to find out the side effects and safety of a combination of the anti-IL23 targeting monoclonal antibody tildrakizumab in combination with abiraterone acetate in men with metastatic castration resistant prostate cancer and to determine the most appropriate dose of this combination. In the Phase I part of this study small groups of patients will be treated with increasing doses of tildrakizumab in combination with a fixed dose of abiraterone acetate (500mg once daily). Once Phase I has been completed the combination with the optimum safety and pharmacokinetic/pharmacodynamic profile will be taken forward to the Phase II part of the study. The Phase II part of the study will evaluate the optimized dose/schedule identified in Phase I of the study in patients with metastatic castration resistant prostate cancer.

Read the detailed description

The trial will be divided into 2 parts: Phase I and Phase II.

The Phase I study will adopt a Bayesian Continual Reassessment Method. Patients will receive single-agent abiraterone run-in of 500 mg orally, once daily (continuous dosing) along with prednisolone at 5 mg BD until PSA progression on abiraterone monotherapy is confirmed. This run-in will not be required if patients have been treated with abiraterone in the previous 6 months. Upon confirmation of PSA progression, tildrakizumab IV will be started and given once every 4-weeks in combination with the fixed dose abiraterone (and prednisolone). The starting dose of tildrakizumab will be 100mg, with single dose escalations to 300mg and 600mg to determine the RP2D to take forward to the Phase II study. Depending on the number of responses observed, dose levels that are deemed tolerable may be expanded to up to a total of 10 patients who are evaluable for response.

The Phase II study will employ a two-stage Minimax design, recruiting up to 25 patients. During the first stage, 15 evaluable patients will be enrolled and followed for a minimum of 2 cycles each. If there are one or more responses confirmed at least 4-weeks later, an additional 10 evaluable patients will be recruited. If 4 or more responses are seen in the 25 patients evaluable for response, the combination will be deemed successful, warranting further evaluation in subsequent phases of testing. In the phase II study, patients will start taking 500mg abiraterone as an oral tablet once daily along with 5mg of prednisolone twice daily until PSA progression on abiraterone monotherapy is confirmed. This run-in will not be required if patients have been treated with abiraterone in the previous 6 months. Upon confirmation of PSA progression, the tildrakizumab will be given as an intravenous infusion at the dose established in the Phase I safety part of the study in combination with the abiraterone (and prednisolone) from combination Cycle 1 Day 1 onwards.

02

Conditions studied

  • Metastatic Castration Resistant Prostate Cancer
03

In context

Lead sponsor

Institute of Cancer Research, United Kingdom is the lead sponsor of 113 studies on the registry; 27 are open to participants now.

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Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Male
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Written (signed and dated) informed consent and be capable of co-operating with treatment and follow-up.
  2. Age 18 or above.
  3. Histologically or cytologically proven adenocarcinoma of the prostate.
  4. Metastatic castration resistant prostate cancer

  5. Documented prostate cancer progression as assessed by the investigator with RECIST (v1.1) and PCWG3 criteria with at least one of the following criteria:

    1. Progression of soft tissue/visceral disease by RECIST (v1.1) and/or,
    2. Progression of bone disease by PCWG3 bone scan criteria and/or,
    3. Progression of PSA by PCWG3 PSA criteria and/or,
    4. Clinical progression with worsening pain and need for palliative radiotherapy for bone metastases.
  6. Patients that have progressed after either enzalutamide or abiraterone treatment (having received a minimum of 12-weeks of enzalutamide or abiraterone).
  7. Ongoing androgen deprivation with a luteinizing hormone releasing hormone analogue (unless the patient is surgically castrated) maintaining serum testosterone of less than 50 ng/dL (less than 2.0 nM) is mandatory.
  8. Life expectancy of at least 12-weeks.
  9. World Health Organisation (WHO) performance status of 0-2
  10. Able to swallow the study drug.
  11. Archival tissue must be available for research analysis.
  12. Patients must have disease that is amenable to biopsy and must be willing to undergo tumour biopsies.
  13. Haematological and biochemical indices within the required ranges in protocol. These measurements must be performed within two weeks prior to the patient's first dose of any investigational medicinal products (IMP).

Exclusion criteria

Exclusion Criteria:

  1. Patients with predominantly small cell or neuroendocrine differentiated prostate cancer are not eligible.
  2. Prior therapy, including major surgery, chemotherapy, radium-223, or other anti-cancer therapy within 4-weeks prior to IMP administration. Patients who were receiving abiraterone acetate (Zytiga® or Yonsa™) immediately prior to trial entry will not need to undergo a washout period. The use of bisphosphonates or RANK ligand inhibitors, provided the patient has been on a stable dose without any dose adjustment for at least 30 days prior to combination Cycle 1 Day 1, in patients with known osteopenia or osteoporosis or bone metastases is permitted. A single fraction of palliative radiation is permitted if at least 14-days before starting trial treatment.

  3. Prior hormonal treatment exclusions as follows:

    • prior flutamide treatment during previous four-weeks N.B. Patients whose PSA did not decline in response to antiandrogens given as a second line or later intervention will only require a 14-day washout;
    • prior bicalutamide (Casodex) and nilutimide (Nilandron) treatment during previous six-weeks;
    • prior progesterone, medroxyprogesterone, progestins, cyproterone acetate, tamoxifen, and 5-alpha reductase inhibitors during previous two-weeks (14-days).
  4. Live vaccine within 4 weeks of starting trial treatment and up to 17 weeks from the last dose of Tildrakizumab.
  5. Prior limited field radiotherapy within the previous two weeks (14-days), or wide field radiotherapy within the previous four weeks of trial entry.
  6. Participation in another interventional clinical trial and any concurrent treatment with any investigational drug within four weeks prior to IMP administration.
  7. Any toxicities due to prior chemotherapy and/or radiotherapy that have not resolved to NCI-CTCAE v5.0 Grade ≤1 with the exception of chemotherapy induced alopecia and Grade 2 peripheral neuropathy.
  8. Clinical evidence of hyperaldosteronism or hypopituitarism.
  9. Use of drugs that are known strong CYP3A4 inducers and CYP2D6 substrates with a narrow therapeutic index (please refer to http://medicine.iupui.edu/clinpharm/ddis/table.aspx). Seville orange or grapefruit products, and any herbal medications should be avoided for four weeks prior to starting trial treatment.
  10. Malabsorption syndrome or other condition that would interfere with enteral absorption of the study drugs.
  11. Known intracerebral metastases

  12. Any of the following cardiac criteria:

    1. QT interval > 470 msec.
    2. Clinically important abnormalities including rhythm, conduction or ECG changes (left bundle branch block, third degree heart block).
    3. Factors predisposing to QT prolongation including congenital long QT syndrome; family history of prolonged QT syndrome, unexplained sudden death (under 40); concomitant medications known to prolong QT interval.
    4. Coronary artery bypass, angioplasty, vascular stent, myocardial infarction, angina or congestive heart failure (NYHA ≥ grade 2) in the last 6 months (see the NYHA scale).
  13. Uncontrolled hypotension (systolic blood pressure \< 90mmHg and or diastolic blood pressure \< 50 mmHg).
  14. Uncontrolled hypertension on optimal medication (systolic blood pressure >180, diastolic blood pressure > 100).
  15. Patients with known history of adrenal insufficiency or mineralocorticoid excess.
  16. Patients with a significant history of liver disease (Child-Pugh B or C, viral or other hepatitis, current alcohol abuse or cirrhosis).
  17. Known history of hepatitis B, hepatitis C or human immunodeficiency virus (HIV).
  18. At high medical risk because of non-malignant systemic disease including active infection, latent or active TB.
  19. Known history of tuberculosis.
  20. Poorly controlled diabetes with HbA1C > 7.5%.
  21. Malignancy other than prostate cancer within three-years of trial entry with the exception of adequately treated basal cell carcinoma. Cancer survivors, who have undergone potentially curative therapy for a prior malignancy must have no evidence of that disease for at least-three years and be deemed at negligible risk for recurrence, are deemed eligible.
  22. Immunocompromised patients including patients who have previously received organ transplants or are on long-term immunosuppression (e.g. corticosteroids of > 10 mg daily equivalent of prednisolone).
  23. Active or uncontrolled autoimmune disease requiring corticosteroid therapy or other forms of systemic immunosuppression.
  24. Any other finding giving reasonable suspicion of a disease or condition that contraindicates the use of an investigational drug or that may affect interpretation of the results or renders the patients at high risk from treatment complications e.g. patients with a hypersensitivity to tildrakizumab, abiraterone, prednisolone, or any of the drug excipients.

  25. Patients with female partners of child-bearing potential (unless they agree to take measures not to father children by using a barrier method of contraception [condom plus spermicide] or to sexual abstinence effective from the first administration of any of the study drugs throughout the trial and for six months afterwards. Men with partners of child-bearing potential must also be willing to ensure that their partner uses an effective method of contraception for the same duration for example, hormonal contraception, intrauterine device, diaphragm with spermicidal gel or sexual abstinence). Men with pregnant or lactating partners must be advised to use barrier method contraception (for example, condom plus spermicidal gel) to prevent exposure of the foetus or neonate.

    NB. Abstinence is only considered to be an acceptable method of contraception when this is in line with the preferred and usual lifestyle of the participants. Periodic abstinence (e.g., calendar, ovulation, sympathothermal, post-ovulation methods) and withdrawal are not acceptable methods of contraception

  26. Prior bone marrow transplant.
  27. Extensive radiotherapy to greater than 25% of bone marrow within 8 weeks.
  28. Any other condition, which in the Investigator's opinion would not make the patient a good candidate for the clinical trial.
  29. Symptoms of COVID-19 and/or documented COVID-19 infection
05

Study design

Phase
Phase 1 / Phase 2
Primary purpose
Health services research
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
13 participants (actual)

Study arms

  • Experimental
    Phase I

    Increasing doses of tildrakizumab in combination with a fixed dose of abiraterone to establish the recommended phase II dose in patients with metastatic castration resistant prostate cancer..

    Drug: Abiraterone Acetate · Drug: Tildrakizumab

  • Experimental
    Phase II

    The Phase II part of the study will evaluate the recommended phase II dose identified in Phase I of the study in patients with metastatic castration resistant prostate cancer.

    Drug: Abiraterone Acetate · Drug: Tildrakizumab

Interventions

  • DrugAbiraterone Acetate

    Supplied as 125 mg tablets

    Also known as: Yonsa

  • DrugTildrakizumab

    Tildrakizumab will be supplied in single-use 100 mg/mL glass vials intended for IV infusion.

06

What researchers measure

Primary outcomes

  1. Phase I - To describe the safety and tolerability of abiraterone acetate and tildrakizumab when given in combination. To establish a RP2D for tildrakizumab, in combination with abiraterone.

    To determine a maximum tolerated dose (MTD) of tildrakizumab by establishing the dose at which the DLT rate is as close to the target DLT rate of 15% as possible, in combination with abiraterone at 500 mg OD with prednisolone at 5 mg bid, and is deemed to be tolerable by the Safety Review Committee. This will be the RP2D for tildrakizumab.

    Time frame: 20 months

  2. Phase II - To determine the antitumour activity of tildrakizumab (at RP2D) in combination with abiraterone in men with mCRPC.

    Antitumour activity will be defined by response rate on the basis of the following outcomes. If any of the following occur, patients will be considered to have responded: * PSA decline ≥ 50% criteria confirmed 4-weeks or later and/or, * Confirmed soft tissue objective response by RECIST (v1.1) in patients with measurable disease and/or, * ONLY for patients with detectable circulating tumour cell (CTC) count of ≥ 5/7.5ml blood at baseline, conversion of CTC count to \<5/7.5ml blood nadir.

    Time frame: 12 months

Secondary outcomes

  1. Phase I - To investigate the PD effects of the tildrakizumab and abiraterone combination in men with mCRPC.

    Measuring the impact of the downregulation of IL-23 signaling in tumour, also evaluating the downregulation of androgen receptor (AR), AR splice variants, and AR target genes.

    Time frame: 20 months

  2. Phase I - To characterize the PK profile of the tildrakizumab and abiraterone combination in men with mCRPC - CMax.

    Determine peak plasma concentration (Cmax) of tildrakizumab and abiraterone when dosed together.

    Time frame: 20 months

  3. Phase I - To characterize the PK profile of the tildrakizumab and abiraterone combination in men with mCRPC - T1⁄2.

    Determine the terminal elimination half-life (T1⁄2) of tildrakizumab and abiraterone when dosed together.

    Time frame: 20 months

  4. Phase I - To characterize the PK profile of the tildrakizumab and abiraterone combination in men with mCRPC - AUC

    Determine the area under the plasma concentration versus time curve (AUC) of tildrakizumab and abiraterone when dosed together.

    Time frame: 20 months

  5. Phase I - To identify molecular determinants of response and anti-tumour activity of the combination of tildrakizumab and abiraterone in men with mCRPC.

    Determine biomarkers of response, including but not limited to PTEN loss, MYC amplification, and intra-tumour MDSC counts, in tumour biopsies from responders and non-responders.

    Time frame: 20 months

  6. Phase I - To determine preliminary anti-tumour activity of the tildrakizumab and abiraterone combination in men with mCRPC.

    Response and progression will be determined using the same measures as that described for the primary objective of the Phase II study.

    Time frame: 20 months

  7. Phase I - To evaluate progression-free survival (PFS) in mCRPC patients receiving the tildrakizumab and abiraterone combination.

    PFS will be measured from the date of addition of tildrakizumab to abiraterone to the date of progression as determined by radiological criteria (RECIST v 1.1, PCWG3 bone scan criteria) or unequivocal clinical progression necessitating drug discontinuation (e.g. worsening pain, spinal cord compression, need for other anticancer therapy).

    Time frame: 20 months

  8. Phase I - To estimate the OS in mCRPC patients receiving the combination of tildrakizumab and abiraterone.

    OS will be measured from the date of addition of tildrakizumab to abiraterone to the date of death (whatever cause).

    Time frame: 20 months

  9. Phase II - To evaluate PFS in mCRPC patients receiving the tildrakizumab and abiraterone combination.

    PFS will be measured from the date of addition of tildrakizumab to abiraterone to the date of progression as determined by radiological criteria (RECIST v 1.1, PCWG3 bone scan criteria) or unequivocal clinical progression necessitating drug discontinuation (e.g. worsening pain, spinal cord compression, need for other anticancer therapy).

    Time frame: 12 months

  10. Phase II - To estimate the biochemical anti-tumour activity of tildrakizumab and abiraterone in mCRPC patients - time to PSA progression.

    The time to PSA Progression will be measured from the date of addition of tildrakizumab to abiraterone.

    Time frame: 12 months

  11. Phase II - To estimate the biochemical anti-tumour activity of tildrakizumab and abiraterone in mCRPC patients - duration of PSA decline by ≥ 50%.

    The duration of PSA decline by ≥ 50%, where this is seen in responding patients.

    Time frame: 12 months

  12. Phase II - To estimate the biochemical anti-tumour activity of tildrakizumab and abiraterone in mCRPC patients - maximum PSA decline.

    The maximum PSA decline experienced per patient. This will be measured following the addition of tildrakizumab to abiraterone.

    Time frame: 12 months

  13. Phase II - To estimate the biochemical anti-tumour activity of tildrakizumab and abiraterone in mCRPC patients - maximum percentage of PSA decline.

    The maximum percentage of PSA decline experienced per patient. This will be measured following the addition of tildrakizumab to abiraterone.

    Time frame: 12 months

  14. Phase II - To determine the pattern of radiologic response to tildrakizumab and abiraterone in mCRPC patients.

    Time to radiological progression (RECIST 1.1 \& PCWG3 Bone Scan criteria). Radiologic PFS (rPFS).

    Time frame: 12 months

  15. Phase II - To identify molecular determinants of response and anti-tumour activity of the combination of tildrakizumab and abiraterone in men with mCRPC.

    Determine biomarkers of response, including but not limited to PTEN loss, MYC amplification, and intra-tumour MDSC counts, in tumour biopsies from responders and non-responders.

    Time frame: 12 months

  16. Phase II - To further investigate the PD effects of the tildrakizumab and abiraterone combination in men with mCRPC.

    Measure the impact of the downregulation of IL-23 signaling in tumour, also evaluating the downregulation of androgen receptor (AR), AR splice variants, and AR target genes

    Time frame: 12 months

  17. Phase II - To determine the rate of response based on CTC conversion.

    Rate of CTC conversion from ≥ 5/7.5 ml blood to \< 5/7.5 ml

    Time frame: 12 months

  18. Phase II - To estimate the OS in mCRPC patients receiving the combination of tildrakizumab and abiraterone.

    OS will be measured from the date of addition of tildrakizumab to abiraterone to the date of death (whatever cause).

    Time frame: 12 months

  19. Phase II - To further characterise the safety and tolerability profile of the combination of tildrakizumab and abiraterone in men with mCRPC.

    Causality and grading severity of each adverse event related to the tildrakizumab and abiraterone combination according to the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) Version 5.0

    Time frame: 12 months

Other outcomes

  1. To determine mechanisms of resistance to the combination of tildrakizumab and abiraterone.

    Deregulation, amongst others, of IL-23, STAT proteins, AR, AR splice variants.

    Time frame: 32 months

  2. To assess putative predictive biomarkers of response to this combination.

    Correlate anti-tumour activity of the combination of tildrakizumab and abiraterone with the detection of putative predictive biomarkers of response and resistance in archival tumours, paired fresh tumour biopsies, and plasma samples.

    Time frame: 32 months

07

Study locations

6 sites
  • Bellinzona Hospital
    Bellinzona, Switzerland
  • Cancer Research Centre at Weston Park Hospital
    Sheffield, England S1O 2SJ, United Kingdom
  • Belfast City Hospital
    Belfast, UK, United Kingdom
  • The Royal Marsden Hospital Foundation Trust
    Sutton, UK, United Kingdom
  • Addenbrooke's Hospital
    Cambridge, United Kingdom
  • University Hospitals Southampton NHS Foundation Trust
    Southampton, United Kingdom
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Dec 2020 to primary completion in Apr 2023, 28 months.

How these figures are worked out, and which studies are left out of them.

Registered
Jun 11, 2020
First posted
Jul 7, 2020
StartActual
Dec 1, 2020
Primary completionActual
Apr 1, 2023
CompletionActual
Nov 15, 2023
Last update
Apr 25, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 25, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT04458311
Lead sponsor
Institute of Cancer Research, United Kingdom
Collaborators
Sun Pharmaceutical Industries Limited
Responsible party
Sponsor
First posted
Jul 7, 2020
Start date
Dec 1, 2020
Primary completion
Apr 1, 2023
Completion
Nov 15, 2023
Last update
Apr 25, 2024

Study contacts

Johann De Bono, MD
study director · National Health Service, United Kingdom

Oversight

FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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