Advanced Solid TumorsPhase 1NCT01946789
A Phase 1 Study of the Clinical and Immunologic Effects of ALT-803 in Patients With Advanced Solid Tumors
A Phase 1 study testing ALT-803 in people with Advanced Solid Tumors, run by Altor BioScience at 5 sites in United States.
Trial summary
The proposed clinical trial is a phase I, open-label, multi-center, dose-escalation study of ALT-803 in patients with surgically incurable advanced solid tumors: melanoma, renal cell, non-small cell lung and squamous cell head and neck cancer Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Advanced Solid Tumors
- What is being tested?
- ALT-803
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 26 participants
- Where
- 5 sitesUnited States
- Study dates
- May 2014to Dec 2017
- Phase
- Phase 1
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
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
ENTRY CRITERIA:
DISEASE CHARACTERISTICS:
- Histological or cytological confirmed malignancy in the following disease groups: melanoma that is metastatic or unresectable, non-small cell lung carcinoma, renal cell carcinoma or squamous cell head and neck carcinoma, for which standard curative or palliative measures do not exist or are no longer effective.
- Primary site may be cutaneous or unknown, but mucosal and ocular primaries are excluded.
- Patients with non-small lung cancer must have had prior EGFR and ALK testing. Patients with sensitizing mutations in EGFR or ALK rearrangements should have been treated with prior targeted agents and have had progression or discontinued due to toxicity from these agents.
- No patients with known brain metastases.
PRIOR/CONCURRENT THERAPY:
- At least one prior therapy using an agent with the potential for prolonged remission.
- Patients with BRAF v600 mutation should be excluded or may be included after experiencing progression following treatment with BRAF inhibitor regimen or if they consent to forgo FDA-approved therapies that increase median survival.
- At least 4 weeks from last dose of prior chemotherapy or immunomodulator therapy with full recovery of acute toxicities. For patients coming off molecularly-targeted therapy, at least 2 weeks since last dose and recovery from laboratory and constitutional toxicities.
- At least 2 weeks from completion of prior radiation therapy with full recovery from toxicities.
- At least 4 weeks from last dose of prior investigational therapy with recovery to meet baseline eligibility criteria.
- Not receiving any current anticancer therapy
- No patients who have had chemotherapy, targeted therapy, or radiotherapy and have not recovered from acute toxicity to their pretreatment baseline or to a grade 1 level within 4 weeks (6 weeks for nitrosoureas or mitomycin C) prior to entering the study. For resolution of autoimmune toxicity from prior immune therapy, patients must be off steroids for at least 30 days without relapse of autoimmune toxicity, or it must be at least 30 days from their last dose of infliximab or related immunosuppressive therapy without relapse of autoimmune toxicity.
- No patients who are receiving any other investigational agents.
- No patients who are receiving chronic systemic or regular inhaled corticosteroid use within 7 days prior to initiation of protocol therapy.
- No immunosuppressive therapy within 30 days prior to treatment start.
PATIENT CHARACTERISTICS
- Age >18 years
- Both men and women of all races and ethnic groups are eligible.
Performance Status
- ECOG performance status ≤1
- Life expectancy of greater than 6 months.
Bone Marrow Function
- leukocytes ≥3,000/mcL
- absolute lymphocyte count ≥500/mcL
- absolute neutrophil count ≥1,000/mcL (without hematopoietic growth factors)
- platelets ≥100,000/mcL (without transfusion)
- hemoglobin ≥ 10 gm/dL (may be transfused but must be stable without clinical evidence of ongoing blood loss or hemolysis)
Hepatic Function
- total bilirubin within normal institutional limits
- AST(SGOT)/ALT(SGPT) ≤2.5 × institutional upper limit of normal
Kidney Function
- Creatinine within normal institutional limits OR
- Creatinine clearance ≥60 mL/min/1.73 m2 for patients with creatinine levels above institutional normal.
Pulmonary Function
- No history of severe COPD or emphysema or interstitial lung disease currently on home supplemental oxygen. Patients with NSCLC with stable COPD or emphysema not requiring supplemental oxygen are eligible.
Cardiac Function
- No symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia. Patients who have underlying risk factors for cardiac disease should be excluded or undergo clearance stress-based cardiac function testing. The pre-treatment QTc must be <500 msec.
- No class II or greater congestive heart failure as described in the New York Heart Association Functional Classification criteria or serious arrhythmias likely to increase the risk of cardiac complications of cytokine therapy.
Other
- Women of child-bearing potential and men must agree to use adequate contraception.
- Ability to understand and the willingness to sign a written informed consent document.
- No uncontrolled inter-current illness or psychiatric illness/social situations that would limit compliance with study requirements.
- No pregnant women.
- No HIV-positive patients.
- No positive hepatitis C serology or active hepatitis B infection.
- No active bacterial or fungal infection.
- No inability to home monitor blood pressure.
- Patients with thyroid disease should be excluded unless euthyroid on suppressive or replacement therapy.
Trial locations and contacts
5 sites in 1 country.
5 sites in 1 country
United States5 sites
Cleveland Clinic Foundation
Cleveland, Ohio, 44195
Dartmouth Hitchcock Medical Center
Lebanon, New Hampshire, 03756
University of Minnesota
Minneapolis, Minnesota, 55455
Rutgers Cancer Institute of New Jersey
New Brunswick, New Jersey, 08901
University of Washington, Seattle Cancer Care Alliance
Seattle, Washington, 98109
About this study
Official title: A Phase 1 Study of the Clinical and Immunologic Effects of ALT-803, a Novel Recombinant IL-15 Complex in Patients With Advanced Solid Tumors: Melanoma, Renal Cell, Non-Small Cell Lung and Squamous Cell Head and Neck Cancer
The proposed clinical trial is a phase I, open-label, multi-center, dose-escalation study of ALT-803 in patients with surgically incurable advanced solid tumors: melanoma, renal cell, non-small cell lung and squamous cell head and neck cancer
Read the detailed description
This trial will investigate the safety and immunogenicity, immunomodulatory properties, and clinical benefits of treatment with weekly doses of ALT-803 in patients with advanced solid tumors.
- Conditions
- Advanced Solid Tumors
- Being tested
- ALT-803
- Keywords
- cancer, IL-15, melanoma, metastatic, unresectable, solid tumors, renal cell, non-small cell lung, squamous cell head and neck
- Medical subject headings
- Neoplasms, Melanoma, Neoplasm Metastasis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
ALT-803Biological
N-803 will be administered at the following doses intravenously: 0.3/0.5, 1.0, 3.0, 6.0 ug/kg N-803 will be administered at the following does subcutaneously: 6.0, 10.0, 15.0, 20.0 ug/kg N-803 will be administered intratumorally at a dose of 10.0 ug/kg, followed by N-803 administered subcutaneously at a dose of 15.0 ug/kg. Each treatment cycle consists of 4 weeks on therapy and 2 weeks off. Patients will receive weekly dose of ALT-803 for 4 weeks (Days 1, 8, 15, and 22) used for the identification of the OBD and MTD. After a 2-week rest period (Weeks 5 and 6) and recovery of any dose limiting toxicities to grade 0-1 of Cycle 1, a second 6-week cycle (4 weeks on treatment and 2 weeks off) can begin. After a rest period during Weeks 5 and 6 of Cycle 2, stable or benefitting patients assessed at week 8 +/- 1 may receive up to 2 additional 6-week cycles.
| Study group | Role | What they receive |
|---|---|---|
| N-803 IV 0.3/0.5 ug/kg | Experimental | Not described Receives: Biological: ALT-803 |
| N-803 IV 1.0 ug/kg | Experimental | Not described Receives: Biological: ALT-803 |
| N-803 IV 3.0 ug/kg | Experimental | Not described Receives: Biological: ALT-803 |
| N-803 IV 6.0 ug/kg | Experimental | Not described Receives: Biological: ALT-803 |
| N-803 Subcutaneous 6.0 ug/kg | Experimental | Not described Receives: Biological: ALT-803 |
| N-803 Subcutaneous 10.0 ug/kg | Experimental | Not described Receives: Biological: ALT-803 |
| N-803 Subcutaneous 15.0 ug/kg | Experimental | Not described Receives: Biological: ALT-803 |
| N-803 Subcutaneous 20.0 ug/kg | Experimental | Not described Receives: Biological: ALT-803 |
| N-803 Intratumoral 10.0 ug/kg followed by N-803 15.0 ug/kg subcutaneous | Experimental | Not described Receives: Biological: ALT-803 |
What is being measured
The primary outcome is the main question the study is designed to answer.
Dose Limiting Toxicity
The safety endpoint is the MTD of ALT-803, defined as the dose level below that at which ≥2 of 6 patients experience a DLT.
Measured: 9 months
Secondary outcomes (6)
Number of Participants Who Developed Anti-drug Antibodies to ALT-803
Immunogenicity of ALT-803 assessed by ELISA
Measured: 14 days post final dose, up to 135 days
To Evaluate the Effect of Escalating Doses of ALT-803: Pharmacokinetics (Half Life and Tmax)
Pharmacokinetics of ALT-803 assessed by ELISA
Measured: 24 hours post dose
To Evaluate the Effect of Escalating Doses of ALT-803: Pharmacokinetics (Cmax)
Pharmacokinetics of ALT-803 assessed by ELISA
Measured: 24 hours after first dose
To Evaluate the Effect of Escalating Doses of ALT-803: Pharmacokinetics (AUC 0-t, AUC0-24, AUC0-infinity)
Pharmacokinetics of ALT-803 assessed by ELISA
Measured: 24 hours after first dose
To Evaluate the Effect of Escalating Doses of ALT-803: Interferon Gamma (IFN-γ)
The level of immune response to autochthonous viral and tumor antigens by interferon gamma (IFN-γ) ELISPOT
Measured: Cycle 1 Week 1, pre-dose; Cycle 1 Week 1, 30 minutes post dose; Cycle 1 Week 1, 2 hours post dose; Cycle 1 Week 1, 4 hours post dose; Cycle 1 Week 1, 8 hours post dose; Cycle 1 Week 1, 24 hours post dose
Objective Response Rate
Number of patients with CR, PR, SD, and PD
Measured: Up to 6 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted20 Sep 2013 (estimated)
- Study startMay 2014
- Primary completionAug 2017
- Study completionDec 2017
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Other trials for Advanced Solid TumorsStudies 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 1
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 26 participants (actual)
Sponsor and investigators
- Lead sponsor
- Altor BioScience
- Sponsor type
- Industry (pharma, biotech, devices)
- Collaborators
- National Cancer Institute (NCI)
- Responsible party
- Sponsor
- Investigators
- Marc Ernstoff, MD, Principal investigator, Roswell Park Cancer Institute
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01946789
- Sponsor's protocol ID
- CITN06-ALT-803, QUILT-3.003
- Other IDs
- U01CA154967
- Status last verified
- Jan 2025
- First submitted
- 11 Sep 2013
- Last updated
- 22 Jan 2025
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- Yes
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 22 Jan 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Phase 1 Study of the Clinical and Immunologic Effects of ALT-803, a Novel Recombinant IL-15 Complex in Patients With Advanced Solid Tumors: Melanoma, Renal Cell, Non-Small Cell Lung and Squamous Cell Head and Neck Cancer
- ClinicalTrials.gov ID
- NCT01946789
- Acronym / sponsor ID
- CITN06-ALT-803, QUILT-3.003
- Conditions
- Advanced Solid Tumors
- Keywords
- cancer, IL-15, melanoma, metastatic, unresectable, solid tumors, renal cell, non-small cell lung
- Phase
- Phase 1
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 26 participants (actual)
- Lead sponsor
- Altor BioScienceIndustry (pharma, biotech, devices)
- Collaborators
- National Cancer Institute (NCI)
- Study start
- May 2014 (actual)
- Primary completion
- Aug 2017 (actual)
- Study completion
- Dec 2017 (actual)
- First posted
- 20 Sep 2013 (estimated)
- Results
- Posted 22 Jan 2025
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The proposed clinical trial is a phase I, open-label, multi-center, dose-escalation study of ALT-803 in patients with surgically incurable advanced solid tumors: melanoma, renal cell, non-small cell lung and squamous cell head and neck cancer
Detailed description
This trial will investigate the safety and immunogenicity, immunomodulatory properties, and clinical benefits of treatment with weekly doses of ALT-803 in patients with advanced solid tumors.
Study design
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 9
| Arm | Type | Receives |
|---|---|---|
| N-803 IV 0.3/0.5 ug/kg | Experimental | Biological: ALT-803 |
| N-803 IV 1.0 ug/kg | Experimental | Biological: ALT-803 |
| N-803 IV 3.0 ug/kg | Experimental | Biological: ALT-803 |
| N-803 IV 6.0 ug/kg | Experimental | Biological: ALT-803 |
| N-803 Subcutaneous 6.0 ug/kg | Experimental | Biological: ALT-803 |
| N-803 Subcutaneous 10.0 ug/kg | Experimental | Biological: ALT-803 |
| N-803 Subcutaneous 15.0 ug/kg | Experimental | Biological: ALT-803 |
| N-803 Subcutaneous 20.0 ug/kg | Experimental | Biological: ALT-803 |
| N-803 Intratumoral 10.0 ug/kg followed by N-803 15.0 ug/kg subcutaneous | Experimental | Biological: ALT-803 |
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 |
|---|---|---|
| ALT-803N-803 will be administered at the following doses intravenously: 0.3/0.5, 1.0, 3.0, 6.0 ug/kg N-803 will be administered at the following does subcutaneously: 6.0, 10.0, 15.0, 20.0 ug/kg N-803 will be administered intratumorally at a dose of 10.0 ug/kg, followed by N-803 administered subcutaneously at a dose of 15.0 ug/kg. Each treatment cycle consists of 4 weeks on therapy and 2 weeks off. Patients will receive weekly dose of ALT-803 for 4 weeks (Days 1, 8, 15, and 22) used for the identification of the OBD and MTD. After a 2-week rest period (Weeks 5 and 6) and recovery of any dose limiting toxicities to grade 0-1 of Cycle 1, a second 6-week cycle (4 weeks on treatment and 2 weeks off) can begin. After a rest period during Weeks 5 and 6 of Cycle 2, stable or benefitting patients assessed at week 8 +/- 1 may receive up to 2 additional 6-week cycles. | Biological | N-803 IV 0.3/0.5 ug/kg, N-803 IV 1.0 ug/kg, N-803 IV 3.0 ug/kg, N-803 IV 6.0 ug/kg, N-803 Intratumoral 10.0 ug/kg followed by N-803 15.0 ug/kg subcutaneous, N-803 Subcutaneous 10.0 ug/kg, N-803 Subcutaneous 15.0 ug/kg, N-803 Subcutaneous 20.0 ug/kg, N-803 Subcutaneous 6.0 ug/kg |
Primary outcome
Dose Limiting Toxicity
Time frame: 9 months
The safety endpoint is the MTD of ALT-803, defined as the dose level below that at which ≥2 of 6 patients experience a DLT.
6 secondary outcomes
Number of Participants Who Developed Anti-drug Antibodies to ALT-803
Time frame: 14 days post final dose, up to 135 days
To Evaluate the Effect of Escalating Doses of ALT-803: Pharmacokinetics (Half Life and Tmax)
Time frame: 24 hours post dose
To Evaluate the Effect of Escalating Doses of ALT-803: Pharmacokinetics (Cmax)
Time frame: 24 hours after first dose
To Evaluate the Effect of Escalating Doses of ALT-803: Pharmacokinetics (AUC 0-t, AUC0-24, AUC0-infinity)
Time frame: 24 hours after first dose
To Evaluate the Effect of Escalating Doses of ALT-803: Interferon Gamma (IFN-γ)
Time frame: Cycle 1 Week 1, pre-dose; Cycle 1 Week 1, 30 minutes post dose; Cycle 1 Week 1, 2 hours post dose; Cycle 1 Week 1, 4 hours post dose; Cycle 1 Week 1, 8 hours post dose; Cycle 1 Week 1, 24 hours post dose
Objective Response Rate
Time frame: Up to 6 months
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 22 Jan 2025.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Related InfoLink provided by the sponsor.
- Individual participant dataSharing planned: Undecided
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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.
Marc Ernstoff, MD principal investigator
Roswell Park Cancer Institute
5 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 ALT-803 in people with Advanced Solid Tumors, run by Altor BioScience at 5 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 22 Jan 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 5 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?
Yes. Results are posted in the registry (first posted 22 Jan 2025). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
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?
Dose Limiting Toxicity (time frame: 9 months). 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 22 Jan 2025.