Non-muscle Invasive Bladder CancerPhase 2ENHANCENCT06503614
A Trial of Durvalumab (MEDI4736) Plus Monalizumab in Non-Muscle-Invasive Bladder Cancer
A Phase 2 study testing Durvalumab and Monalizumab in people with Non-muscle Invasive Bladder Cancer and Non-Muscle Invasive Bladder Urothelial Carcinoma, run by John Sfakianos at 5 sites in United States.
Trial summary
This is a phase 2 open-label two cohort study of durvalumab plus monalizumab in patients with BCG-unresponsive or BCG-exposed CIS NMIBC. Arm A will enroll 43 participants who have cancer in situ (CIS) with or without high grade papillary urothelial cancer. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Non-muscle Invasive Bladder Cancer, Non-Muscle Invasive Bladder Urothelial Carcinoma
- What is being tested?
- Durvalumab and Monalizumab
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 60 participants
- Where
- 5 sitesUnited States
- Study dates
- 24 Feb 2025to 22 Dec 2032
- Phase
- Phase 2
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
Who may be able to join
- Age ≥18 years at the time of consent.
- Patient is willing and able to comply with the protocol for the duration of the study including undergoing treatment and scheduled visits and examinations including follow up. Able and willing to provide written informed consent.
- Eastern Cooperative Oncology Group scores ≤ 1 within 28 days prior to registration.
- Non-muscle-invasive bladder cancer
- Cohort A: CIS +/- high grade papillary urothelial cancer (Ta or T1) after 3-mo evaluation after induction BCG.
- Cohort B: High grade papillary urothelial cancer (Ta or T1) after 3-mo evaluation after induction BCG.
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- Mixed variant histology (adenocarcinoma, squamous cell carcinoma) is eligible, but pure variant histology is ineligible. NOTE: Pathology report required for documentation purposes.
- Patients can have BCG-unresponsive or BCG-exposed NMIBC11. Adequate BCG therapy is defined as completing at least induction BCG (≥ 5 doses) and the first round of maintenance or second induction course BCG (≥ 2 doses). The subsequent round of BCG, either maintenance or repeat induction, must be given within 6 months of initial induction BCG.
- BCG-unresponsive is defined as high grade persistent or recurrent NMIBC that has not achieved a disease-free status after an adequate course of BCG therapy. This includes patients with:
- Persistent or recurrent high-grade tumors (Ta/T1) or carcinoma in situ (CIS) within 6 to 12 months of completing adequate BCG therapy.
- Recurrent high-grade papillary disease within 6 months of BCG therapy.
- High-grade T1 disease found at the first evaluation after BCG induction therapy alone.
- BCG-exposed is defined as high grade NMIBC that has recurred after an initial response or is still present after initial treatment, but recurrence is never too late to be considered "BCG-unresponsive". This includes patients with:
- High-grade recurrence between 12 and 24 months after adequate BCG therapy.
- Recurrence within 24 months of inadequate BCG therapy.
- High-risk recurrence at the 3-month mark after an initial BCG induction.
- High grade recurrence (T1, Ta, CIS) while on maintenance therapy would be eligible. The recurrence must be within 6 months of the last BCG dose.
- Patients may have received up to 2 lines of prior therapy (including chemotherapy or other approved agents) for NMIBC (NOTE: prior PD-1/PD-L1 blockade is prohibited).
- Patients must be deemed unfit for radical cystectomy by the treating physician or refuse radical cystectomy. NOTE: Reason for being deemed unfit or refusal should be documented in the medical record.
- All visible tumor must be completely resected within 60 days prior to registration (residual pure CIS is permitted).
- All patients must have had a cystoscopy (or TURBT with complete resection) without papillary tumor and negative urine cytology within 28 days prior to registration (positive cytology is allowed in patients with CIS).
- All patients with T1 tumors must undergo restaging TURBT within 60 days prior to registration.
- There must be uninvolved muscularis propria in the restaging TURBT specimen.
- The initial TURBT prior to the restaging TURBT may be > 60 days prior to registration.
- Patients must have baseline tumor tissue from either initial or repeat TURBTs for submission of a minimum of 2 and up to 10 unstained slides for translational study objectives. If archival tissue is not available, the subject is not eligible.
- Adequate organ function as defined by ALL of the following within 28 days prior to registration:
- Absolute neutrophil count ≥ 1500/µL
- Platelets ≥ 100,000/µL
- Hemoglobin ≥ 9 g/dL
- Aspartate aminotransferase/alanine aminotransferase ≤ 1.5× upper limit of normal (ULN)
- Total serum bilirubin ≤ 1.5×ULN*; *Patients with Gilbert's disease: ≤ 3×ULN
- International normalized ratio (INR) and activated partial thromboplastin time (aPTT) ≤ 1.5×ULN unless the patient is on therapeutic anticoagulation.
- Creatinine clearance ≥ 40 mL/min by Cockcroft-Gault estimation. The patient's estimated CrCl will be calculated by the local laboratory (for eligibility purposes) using screening/baseline age, actual weight (kg), and serum creatinine:
- Males: CrCl = ((140 - age in years) × weight (kg)) / (72× serum creatinine (mg/dL)) Females: CrCl = ((140 - age in years) × weight (kg) ×0.85) / (72× serum creatinine (mg/dL))
- Females of childbearing potential (FOCBP) must have a negative urine or serum pregnancy test within 7 days of registration. If a urine test is done and it is positive or cannot be confirmed as negative, a serum pregnancy test will be required. FOCBP must agree to use contraception during the study.
- Men capable of fathering a child must agree to use contraception during the study.
- Must have a life expectancy of at least 12 weeks.
Who cannot join
- Prior therapy with an anti-PD-1, anti-PD-L1, or anti PD L2 agent or with an agent directed to another stimulatory or co-inhibitory T-cell receptor (e.g., CTLA-4, OX 40, CD137).
- Prior CIS of the ureters or prostatic urethra within 24 months prior to registration.
- Evidence of metastatic disease on imaging (CT or MRI) of the abdomen and pelvis within 90 days of registration.
- Body weight ≤ 30 kg.
- History of allogeneic organ transplantation.
- History of another primary malignancy other than muscle-invasive bladder cancer less than 5 years prior to Day 1 of this trial, with the exception of a malignancy treated with curative intent and with no known active disease ≥ 5 years before the first dose of study drug and of low potential risk for recurrence. Other exceptions include those with a negligible risk of metastasis or death and with expected curative outcome (such as adequately treated carcinoma in situ of the cervix, basal or squamous cell skin cancer (non-melanoma skin cancer) or lentigo maligna without evidence of disease, localized prostate cancer treated surgically with curative intent, or ductal carcinoma in situ without evidence of disease treated surgically with curative intent) or undergoing active surveillance per standard-of-care management (e.g., chronic lymphocytic leukemia Rai Stage 0, prostate cancer with Gleason score ≤ 6, and prostate specific antigen [PSA] ≤ 10 mg/mL, etc.)
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- Currently participating in or has participated in a trial of an investigational agent within 4 weeks prior to the first dose of study treatment or 5 half-lives, whichever is longer without recovery of clinically significant toxicities from that therapy.
- Active or prior autoimmune or inflammatory disorders requiring systemic treatment within 24 months prior to registration. Autoimmune or inflammatory disorders include, but not limited to, systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease(colitis or Crohn's disease), diverticulitis (with the exception of diverticulosis),antiphospholipid syndrome, Sarcoidosis syndrome, or Wegener's syndrome (granulomatosis with polyangiitis, Graves' disease, hypophysitis, uveitis, etc), Sjogren's syndrome, Bell's palsy, Guillain-Barre syndrome, multiple sclerosis, autoimmune thyroid disease, vasculitis, or glomerulonephritis. NOTE: The following are exceptions to this criterion: Patients with vitiligo or alopecia, hypothyroidism (e.g., following Hashimoto syndrome) stable on hormone replacement. Any chronic skin condition that does not require systemic therapy. Patients without active disease in the last 5 years may be included but only after consultation with the study physician. Patients with celiac disease controlled by diet alone.
- A diagnosis of immunodeficiency or is receiving chronic systemic steroid therapy (in dosing exceeding 10 mg daily of prednisone equivalent) or any other form of immunosuppressive therapy within 7 days prior to registration. NOTE: Replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency) is not considered a form of systemic treatment and is allowed.
- Known psychiatric or substance abuse disorder that would interfere with the participant's ability to cooperate with the requirements of the study.
- Active known tuberculosis.
- Symptomatic herpes zoster within the past 30 days.
- Active infection requiring systemic therapy. NOTE: Prophylactic antibiotics are permitted. Treatment for a UTI is allowed but must be deemed adequately treated by the treating physician prior the start of C1D1.
- History of idiopathic pulmonary fibrosis or organizing pneumonia.
- History of (non-infectious) pneumonitis that required steroids or have current pneumonitis.
- Patients known to have tested positive for human immunodeficiency virus (HIV) (positive HIV 1/2 antibodies) are eligible with the following:
- On effective anti-retroviral therapy with undetectable viral load within 6 months of registration.
- HIV-infected participants must not have a history of Kaposi sarcoma and/or Multicentric Castleman Disease.
- Known active hepatitis infection, positive hepatitis C virus (HCV) antibody, hepatitis B virus (HBV) surface antigen (HBsAg) or HBV core antibody (anti-HBc), at screening. Participants with a past or resolved HBV infection (defined as the presence of anti HBc and absence of HBsAg) are eligible. Participants positive for HCV antibody are eligible only if polymerase chain reaction is negative for HCV RNA. NOTE: No testing for Hepatitis B and Hepatitis C is required unless mandated by a local health authority.
- Participants with a known co-infection with HBV and HCV, or co-infection with HBV and HDV, namely: HBV positive (presence of HBsAg and/or anti HBcAb with detectable HBV DNA); AND HCV positive (presence of anti-HCV antibodies); OR HDV positive (presence of anti-HDV antibodies).
- Known allergy or hypersensitivity to any of the study drugs or any of the study drug excipients.
- Received live vaccines within 30 days of study treatment. Examples of live vaccines include, but are not limited to, the following: measles, mumps, rubella, varicella/zoster (chicken pox), yellow fever, rabies, Bacillus Calmette-Guérin (BCG), and typhoid vaccine. Seasonal influenza vaccines for injection are generally killed virus vaccines and are allowed; however, intranasal influenza vaccines (e.g., FluMist®) are live attenuated vaccines and are not allowed. COVID-19 vaccinations are permitted.
- Major surgical procedure (as defined by the Investigator) within 28 days prior to the first dose of study drug. Note: Local surgery of isolated lesions for palliative intent is acceptable.
- Uncontrolled intercurrent illness, including but not limited to, symptomatic congestive heart failure, uncontrolled hypertension, unstable angina pectoris, cardiac arrhythmia, interstitial lung disease, serious chronic gastrointestinal conditions associated with diarrhea, or psychiatric illness/social situations that would limit compliance with study requirement, substantially increase risk of incurring AEs or compromise the ability of the patient to give written informed consent.
- Mean QT interval corrected for heart rate using Fridericia's formula (QTcF) ≥470 ms calculated from 3 ECGs (within 15 minutes at 5 minutes apart).
- Female patients who are pregnant or breastfeeding or male or female patients of reproductive potential who are not willing to employ effective birth control.
- Any unresolved toxicity NCI CTCAE Grade ≥2 from previous anticancer therapy with the exception of alopecia, vitiligo, and the laboratory values defined in the inclusion criteria
- Patients with Grade ≥2 neuropathy will be evaluated on a case-by-case basis after consultation with the Study Physician.
- Patients with irreversible toxicity not reasonably expected to be exacerbated by treatment with durvalumab may be included only after consultation with the Study Physician.
- Any concurrent chemotherapy, IP, biologic, or hormonal therapy for cancer treatment. Concurrent use of hormonal therapy for non-cancer-related conditions (e.g., hormone replacement therapy) is acceptable.
- History of leptomeningeal carcinomatosis
- Prior randomization or treatment in a previous durvalumab clinical study regardless of treatment arm assignment.
- Current or prior use of immunosuppressive medication within 14 days before the first dose of durvalumab. The following are exceptions to this criterion:
- Intranasal, inhaled, topical steroids, or local steroid injections (e.g., intra articular injection)
- Systemic corticosteroids at physiologic doses not to exceed <<10 mg/day>> of prednisone or its equivalent
- Steroids as premedication for hypersensitivity reactions (e.g., CT scan premedication
Trial locations and contacts
5 sites in 1 country. Contact the study team or a site near you to ask about taking part.
5 sites in 1 country
United States5 sites, 5 recruiting
- Recruiting
Rutgers Cancer Institute of New Jersey
New Brunswick, New Jersey, 08903
Alicia Alexander-Moore, 732-235-9850, aca108@cinj.rutgers.edu
Saum Ghodoussipour, MD
- Recruiting
Icahn School of Medicine at Mount Sinai
New York, New York, 10029
Lindsay Diamond, lindsay.diamond@mssm.edu
John P Sfakianos, MD
- Recruiting
Weill Cornell Medical Center
New York, New York, 10065
Amalia Korniyenko, 646-962-9406, nak4026@med.cornell.edu
Douglas Scherr, MD
- Recruiting
University of California San Francisco
San Francisco, California, 94158
Angela Mak, CRC, 415-699-6023, angela.mak@ucsf.edu
Vadim Koshkin, MD
- Recruiting
Moffitt Cancer Center
Tampa, Florida, 33612
Arfa Mustasam, MBBS, CCRP, 813-745-7272, Arfa.Mustasam@moffitt.org
Juskaran Chadha, DO
About this study
Official title: ENHANCE (Elevated NKG2A and HLA-E Amplify NK/CD8 Checkpoint Engagers): A Phase 2 Trial of Durvalumab (MEDI4736) Plus Monalizumab in Non-Muscle-Invasive Bladder Cancer
This is a phase 2 open-label two cohort study of durvalumab plus monalizumab in patients with BCG-unresponsive or BCG-exposed CIS NMIBC. Arm A will enroll 43 participants who have cancer in situ (CIS) with or without high grade papillary urothelial cancer. Arm B will enroll 17 participants who do not have cancer in situ (CIS) but do have high grade papillary urothelial cancer. Eligible patients will be enrolled to receive up to 13 cycles of monthly combination of monalizumab and durvalumab. Both monalizumab and durvalumab will be administered intravenously (IV) every 28 days.
- Being tested
- Durvalumab, Monalizumab
- Medical subject headings
- Non-Muscle Invasive Bladder Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
DurvalumabDrug
Also called MEDI 4736
Durvalumab 1500mg IV
MonalizumabDrug
Monalizumab 1500mg IV
| Study group | Role | What they receive |
|---|---|---|
| Cohort A: Durvalumab and Monalizumab for CIS +/- high grade papillary urothelial cancer | Experimental | Durvalumab 1500mg IV and monalizumab 1500mg IV will be administered to all patients once every 4 weeks. A cycle is equal to 4 weeks. This will continue until disease progression, unacceptable toxicity, or for a maximum of 1 year. Receives: Drug: Durvalumab; Drug: Monalizumab |
| Cohort B: Durvalumab and Monalizumab for high grade papillary urothelial cancer without CIS | Experimental | Durvalumab 1500mg IV and monalizumab 1500mg IV will be administered to all patients once every 4 weeks. A cycle is equal to 4 weeks. This will continue until disease progression, unacceptable toxicity, or for a maximum of 1 year. Receives: Drug: Durvalumab; Drug: Monalizumab |
What is being measured
The primary outcome is the main question the study is designed to answer.
Complete Response
Complete response will be determined by bladder biopsy and urinary cytology for malignancy for subjects with a CIS component at 6 months CT/MRI urography will be used to rule out extravesical disease. (Cohort A)
Measured: 6 months
Secondary outcomes (7)
Incidence of treatment related Adverse Events
Safety will be determined by summarizing all treatment related adverse events according to the NCI Common Terminology Criteria for Adverse Events (NCI CTCAE) v5. (Cohort A and B)
Measured: 12 months
Progression-free Survival (PFS)
Progression-free survival (PFS) will be measured from the date of study registration to the date of progression or death due to any cause, whichever occurs first. Surviving patients without any documented progression will be censored at the date of last known contact. Progression will be defined as the development of muscle invasive bladder cancer or metastatic urothelial cancer (nodal and/or distant). (Cohort A)
Measured: 36 months
Overall Survival (OS)
Overall survival (OS) will be measured from the date of study registration to date of death due to any cause. Surviving patients will be censored at the date of last known contact. (Cohort A)
Measured: 36 months
Event Free Survival
Event-free survival will be measured from the date of study registration to the first documentation of an event. Patients without documented events and who are still alive, will be censored at last disease assessment. Patients who start any subsequent anti- cancer therapy without any reported events will be censored at their last disease assessment. (Cohort A)
Measured: 36 months
Cyctectomy Free Survival
Cystectomy-free survival will be measured from the date of study registration to the date of cystectomy for all patients. (Cohort A)
Measured: 36 months
Duration of Response (DOR)
Duration of response (DOR) will be measured from the time a patient had a documented response (the time would start at the time a response was first noted) until disease-progression. This analysis will only include those patients in the CIS population who achieve a response. Patients who are alive and without a documented progression at the time of analysis will be censored at the time of the last disease status evaluation. (Cohort A)
Measured: 36 months
Recurrence-free Survival
Recurrence-free survival will be measured from the date of study registration to the date of recurrence. Recurrence will be defined as the development of high-grade bladder cancer for patients without a CIS component at baseline. (Cohort B)
Measured: 12 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted16 Jul 2024
- Study start24 Feb 2025
- Primary completion22 Dec 2027 (estimated)
- Study completion22 Dec 2032 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Non-muscle Invasive Bladder CancerStudies of the same condition, open and under way.
- 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 2
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 60 participants (estimated)
Sponsor and investigators
- Lead sponsor
- John Sfakianos
- Sponsor type
- University, hospital or other
- Collaborators
- AstraZeneca, Icahn School of Medicine at Mount Sinai, Bladder Cancer Advocacy Network
- Responsible party
- Sponsor-investigator, John Sfakianos, Hoosier Cancer Research Network
- Investigators
- John Sfakianos, MD, Principal investigator, Icahn School of Medicine at Mount Sinai
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06503614
- Sponsor's protocol ID
- HCRN GU21-551
- Acronym
- ENHANCE
- Status last verified
- Sep 2026
- First submitted
- 10 Jul 2024
- Last updated
- 5 Oct 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- Yes
- FDA-regulated device
- No