Platinum Resistant Ovarian CancerPhase 1/2NCT03319628
First-in-Human Study of XMT-1536 in Cancers Likely to Express NaPi2b
A Phase 1/2 study testing upifitamab rilsodotin in people with Platinum Resistant Ovarian Cancer and Non Small Cell Lung Cancer Metastatic, run by Mersana Therapeutics at 1 site in United States.
Trial summary
First-in-human, Phase 1b/2 safety study of the antibody-drug conjugate (ADC) XMT-1536 (upifitamab rilsodotin) administered as an intravenous infusion once every four weeks. Patients with tumor types likely to express NaPi2b were enrolled in dose escalation. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Platinum Resistant Ovarian Cancer, Non Small Cell Lung Cancer Metastatic
- What is being tested?
- upifitamab rilsodotin
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 523 participants
- Where
- 1 siteUnited States
- Study dates
- 12 Dec 2017to 31 Oct 2024
- Phase
- Phase 1/2
- Are there results?
- Not yet: the study is under way
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
General Inclusion Criteria (for Dose Escalation, Expansion, and UPLIFT):
- ECOG performance status 0 or 1
- Measurable disease as per RECIST, version 1.1
- Resolution of all acute toxic effects of prior therapy or surgical procedures to ≤Grade 1 (except alopecia, stable immune-related toxicity such as hypothyroidism on hormone replacement, adrenal insufficiency on ≤10 mg daily prednisone [or equivalent], chronic Grade 2 peripheral sensory neuropathy after prior taxane therapy).
- Cardiac left ventricular ejection fraction (LVEF) ≥50% or ≥ the institution's lower limit of normal by either Echo or MUGA scan
- Adequate organ function as defined by the following criteria:
- Absolute neutrophil count (ANC) ≥1500 cells/mm3
- Platelet count ≥100,000/mm3
- Hemoglobin ≥9 g/dL
- In patients not on anticoagulation therapy: INR, activated partial thromboplastin time (aPTT), and prothrombin time (PT) all within 1.2 times the institution's upper limit of normal (ULN). Patients on anticoagulation therapy are allowed if their relevant laboratory values are within the therapeutic window.
- Estimated glomerular filtration rate (GFR) ≥45 mL/min
- Total bilirubin ≤ULN
- g. Patients with asymptomatic elevations in unconjugated bilirubin due to Gilbert syndrome or stable chronic hemolytic anemia (e.g., hereditary spherocytosis, sickle cell disease, thalassemia intermedia) may be eligible after discussion with the Sponsor Medical Monitor.
- Aspartate aminotransferase (AST or SGOT) and alanine aminotransferase (ALT or SGPT) ≤1.5 times the institutional ULN.
- Albumin ≥3.0 g/dL
- Able to provide informed consent.
General Exclusion Criteria (for Dose Escalation, Expansion, and UPLIFT) :
- Major surgery within 28 days of starting study treatment, systemic anti-cancer therapy within the lesser of 28 days or 5 half-lives of the prior therapy before starting study treatment, or recent radiation therapy with unresolved toxicity or within a time window of potential toxicity.
- Patients with untreated CNS metastases (including new and progressive brain metastases), history of leptomeningeal metastasis or carcinomatous meningitis.
- Current known active infection with HIV, hepatitis B virus, or hepatitis C virus.
- Prior history of liver disease such as liver cirrhosis, hepatic fibrosis
- Current severe, uncontrolled systemic disease (e.g., clinically significant cardiovascular, pulmonary, or metabolic disease) or intercurrent illness that could interfere with per-protocol evaluations.
- Current use of either constant or intermittent supplementary oxygen therapy.
- History of suspected pneumonitis or interstitial lung disease.
- Pregnant or nursing women.
- History of other malignancy within the last 2 years, except for appropriately treated carcinoma in situ of the cervix, non-melanoma skin carcinoma, or other malignancy with a similar expected curative outcome.
- Active corneal disease, or history of corneal disease within 12 months prior to enrollment
- Use of strong CYP450 3A inhibitors or inducers that cannot be discontinued while receiving study treatment
- Oxygen saturation on room air <93%
Ovarian Cancer Inclusion Criteria for UPLIFT:
- Histological diagnosis of high grade serous ovarian cancer, which includes fallopian tube, or primary peritoneal cancer, that is metastatic or recurrent.
- Platinum-resistant disease
- Patients who have only had 1 line of platinum-based therapy must have received at least 4 cycles of platinum, must have had a response [complete response/remission (CR) or partial response/remission (PR)], and then progressed between 3 months and ≤ 6 months after the date of the last dose of platinum
- Patients who have received 2 to 4 lines of prior therapy must have received at least 4 cycles of platinum and then progressed within 6 months after the date of the last dose of platinum
- One to 4 prior lines of systemic therapy for ovarian cancer
- Prior treatment with bevacizumab is required for patients with 1 to 2 prior lines of therapy
- Patients must be willing to provide an archival tumor tissue block or slides or if not available, undergo procedure to obtain a new tumor biopsy using a low-risk, medically routine procedure
Ovarian Cancer Exclusion Criteria for UPLIFT:
- Low-grade, clear cell, endometrioid, mucinous, carcinosarcoma, germ-cell, mixed histology, or stromal tumors
- Prior treatment with mirvetuximab soravtansine or another ADC containing an antitubulin payload
- Primary platinum-resistant disease, defined by a lack of response or by progression within 3 months after completing front-line, platinum-containing therapy.
- Participation in DES or EXP segments of this study
Ovarian Cancer Inclusion Criteria for QTc sub-study:
Note: patients must meet all UPLIFT cohort inclusion criteria in order to participate in the QTc sub-study
- Study patient has agreed to remain in the clinic for the additional QTc related study activities on the Day 1 of Cycle 1 and Cycle 3.
Ovarian Cancer Exclusion Criteria for QTc sub-study:
- Use of strong CYP450 3A inducers.
- Uncontrolled cardiac arrhythmias, for example, atrial fibrillation with a ventricular response at rest > 100 beats per minute. left bundle branch block (LBBB)
- Known abnormality of any cardiac valve (either stenosis or regurgitation) that is greater than moderate in severity.
- Subjects not in sinus rhythm at screening with HR >45- <100
- Any ECG abnormality that can interfere with the measurement of the QT interval
Trial locations and contacts
1 site in 1 country.
United States1 site
University of Oklahoma
Oklahoma City, Oklahoma, 73104
About this study
Official title: A Phase 1b/2, First-in-Human, Dose Escalation and Expansion Study of XMT-1536 In Patients With Solid Tumors Likely to Express NaPi2b
First-in-human, Phase 1b/2 safety study of the antibody-drug conjugate (ADC) XMT-1536 (upifitamab rilsodotin) administered as an intravenous infusion once every four weeks. Patients with tumor types likely to express NaPi2b were enrolled in dose escalation. Patients with platinum-resistant ovarian cancer and non-small cell lung cancer (adenocarcinoma subtype) were enrolled in the expansion segment of this study. Patients with platinum-resistant, high-grade serous ovarian cancer were enrolled in the UPLIFT segment of this study. In addition to safety assessments, the pharmacokinetics of the drug were assessed along with ADC activity. A QTc sub-study was added for the UPLIFT cohort for a sub-set of sites.
Read the detailed description
This is a multi-center study of XMT-1536 (upifitamab rilsodotin) in patients with tumors likely to express NaPi2b, focusing on patients with platinum-resistant ovarian cancer and non-small cell lung cancer, adenocarcinoma subtype. XMT-1536 (upifitamab rilsodotin) was administered as an intravenous infusion once every four weeks. The study consisted of three segments: dose escalation (DES), dose expansion (EXP), and the pivotal cohort (UPLIFT). The DES segment studied small groups of patients who received increased doses. A Safety Review Committee was established to review the data from each dose level before moving to the next higher dose. The dose escalation cohort has ended and is no longer enrolling patients. Enrollment into the EXP segment consisted of 2 parallel cohorts of patients to confirm the dose that has been identified in DES and estimate the objective response rate in each patient population. The EXP and UPLIFT cohorts are no longer enrolling patients. All adverse events were graded according to the National Cancer Institute (NCI) Common Terminology Criteria version (CTCAE v5.0). Throughout the study, pharmacokinetics were measured using proprietary assays developed by Mersana. Anti-cancer activity were measured via RECIST.
- Being tested
- upifitamab rilsodotin
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
upifitamab rilsodotinDrug
Also called XMT-1536, UpRi
XMT-1536 will be administered once every 28 days until disease progression, unacceptable toxicity, or either the patient or study physician determines it is in the best interest of the patient to discontinue participation in the study.
For sites participating in the sub-study, patients with platinum -resistant ovarian cancer will have the option to enroll in this sub-study to evaluate potential changes in the QTc interval following administration of XMT-1536
| Study group | Role | What they receive |
|---|---|---|
| Dose Escalation | Experimental | XMT-1536 (upifitamab rilsodotin) treatment is administered in groups of patients who will receive doses that increase over time.
This cohort is closed to enrollment. Receives: Drug: upifitamab rilsodotin |
| Dose Expansion - Ovarian Cancer | Experimental | Once the maximum tolerated dose or recommended Phase 2 dose is achieved in dose escalation, new groups of patients will receive XMT-1536 (upifitamab rilsodotin) at this fixed-dose.
This cohort is closed to enrollment. Receives: Drug: upifitamab rilsodotin |
| Dose Expansion - NSCLC adenocarcinoma | Experimental | Once the maximum tolerated dose or recommended Phase 2 dose is achieved in dose escalation, new groups of patients will receive XMT-1536 (upifitamab rilsodotin) at this fixed-dose.
This cohort is closed to enrollment. Receives: Drug: upifitamab rilsodotin |
| Pivotal Cohort (UPLIFT) | Experimental | Patients with platinum-resistant ovarian cancer will receive XMT-1536 (upifitamab rilsodotin) to further confirm the efficacy.
This cohort is closed to enrollment. Receives: Drug: upifitamab rilsodotin |
| QTc Sub-Study | Experimental | For sites participating in the sub-study, patients with platinum -resistant ovarian cancer will have the option to enroll in this sub-study to evaluate potential changes in the QTc interval following administration of XMT-1536.
This cohort is closed to enrollment. Receives: Drug: upifitamab rilsodotin |
What is being measured
The primary outcome is the main question the study is designed to answer.
DES: Maximum tolerated dose or recommended Phase 2 dose
Evaluate adverse events and concomitant medication use after XMT-1536 (upifitamab rilsodotin) doses
Measured: Up to 36 weeks, from the date of first dose until unacceptable side effects or a dose-limiting toxicity is met
DES and EXP: Safety and Tolerability
Evaluate incidence and severity of adverse events
Measured: First dose up until 30 days after study termination
EXP: Anti-neoplastic effects of XMT-1536 (upifitamab rilsodotin)
Monitor tumor size
Measured: Every 6 weeks for up to 36 weeks
UPLIFT: Investigator-assessed objective response rate (ORR) of XMT-1536 (upifitamab rilsodotin) in the ITT-Higher NaPi2b population
Confirmed ORR is defined as the proportion of patients who have achieved a confirmed complete response (CR) or partial response (PR) per RECIST v1.1 after the initiation of study treatment.
Measured: Every 8 weeks until disease progression or up to 24 months
QTc Sub-study: Evaluation of the concentration response analysis of XMT-1536 versus the change in QTcF values
"The concentration-QTcf change from baseline deltaQTcF analysis and analysis of central tendency for deltaQTcF
Measured: 60 minutes prior to first dose, up to 26 hours after Cycle 3 dose
Secondary outcomes (11)
DES and EXP: Time of maximum observed concentration of XMT-1536 (upifitamab rilsodotin)
Determine the pharmacokinetics of XMT-1536 (upifitamab rilsodotin)
Measured: Daily for one week after first dose; weekly until 28 days after first dose; immediately before and after and 1 week after all subsequent doses
DES and EXP: Maximum concentration of XMT-1536 (upifitamab rilsodotin)
Determine the pharmacokinetics of XMT-1536 (upifitamab rilsodotin)
Measured: Daily for one week after first dose; weekly until 28 days after first dose; immediately before and after and 1 week after all subsequent doses
DES and EXP: Area under the concentration curve of the last measurable concentration of XMT-1536 (upifitamab rilsodotin)
Determine the pharmacokinetics of XMT-1536 (upifitamab rilsodotin)
Measured: Daily for one week after first dose; weekly until 28 days after first dose; immediately before and after and 1 week after all subsequent doses
DES: Anti-neoplastic effects of XMT-1536 (upifitamab rilsodotin)
Monitor tumor size
Measured: Every 6 weeks for up to 36 weeks
DES and EXP: Anti-drug antibody and neutralizing antibody
Analyze blood for antibodies to XMT-1536 (upifitamab rilsodotin) and neutralizing antibodies
Measured: Every 6 weeks for up to 36 weeks
UPLIFT: Confirmed Investigator-assessed objective response rate of XMT-1536 (upifitamab rilsodotin) regardless of NaPi2b expression
Assess the confirmed investigator-assessed objective response rate of XMT-1536 (upifitamab rilsodotin) regardless of NaPi2b expression
Measured: Every 8 weeks until disease progression or up to 24 months
UPLIFT: Confirmed objective response rate by independent radiology review (IRR) for patients with high NaPi2b and overall
Assess the confirmed objective response rate by IRR for patients with high NaPi2b (TPS >/=75) and overall
Measured: Every 8 weeks until disease progression or up to 24 months
UPLIFT: Duration of objective response (DOR)
Assess the duration of objective response (DOR) in patients who achieve a response
Measured: 4 weeks after first response and every 8 weeks until disease progression or up to 24 months
UPLIFT: Incidence and severity of adverse events
Evaluate incidence and severity of adverse events
Measured: First dose up until 60 days after study termination
QTc Sub-Study: Evaluation of the effect of XMT-1536 on QTcF in patients with platinum-resistant HGSOC by timepoint analysis
Con.-QTc evaluation
Measured: 60 minutes prior to first dose, up to 26 hours after Cycle 3 dose
QTc Sub-Study: Evaluation of the effect of XMT-1536 on the PR-interval (PR), QRS duration (QRS), Heart Rate (HR), and ECG morphology
Con.-QTc evaluation
Measured: 60 minutes prior to first dose, up to 26 hours after Cycle 3 dose
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted24 Oct 2017
- Study start12 Dec 2017
- Primary completion31 May 2023
- Study completion31 Oct 2024 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Platinum Resistant Ovarian 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 1/2
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Model description
- Open-label, dose escalation to reach MTD. The MTD will be confirmed in parallel cohorts: patients with platinum-resistant ovarian cancer; patients with non-squamous NSCLC, adenocarcinoma subtype
- Masking
- None (open label)
- Enrolment
- 523 participants (actual)
Sponsor and investigators
- Lead sponsor
- Mersana Therapeutics
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Robert Burger, MD, Study director, Mersana Therapeutics
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03319628
- Sponsor's protocol ID
- XMT-1536-1
- Status last verified
- Sep 2023
- First submitted
- 17 Oct 2017
- Last updated
- 13 Nov 2023
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 13 Nov 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Phase 1b/2, First-in-Human, Dose Escalation and Expansion Study of XMT-1536 In Patients With Solid Tumors Likely to Express NaPi2b
- ClinicalTrials.gov ID
- NCT03319628
- Acronym / sponsor ID
- XMT-1536-1
- Phase
- Phase 1/2
- Study type
- Interventional
- Recruitment status
- Active, not recruiting
- Enrolment
- 523 participants (actual)
- Lead sponsor
- Mersana TherapeuticsIndustry (pharma, biotech, devices)
- Study start
- 12 Dec 2017 (actual)
- Primary completion
- 31 May 2023 (actual)
- Study completion
- 31 Oct 2024 (estimated)
- First posted
- 24 Oct 2017 (actual)
- 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.
First-in-human, Phase 1b/2 safety study of the antibody-drug conjugate (ADC) XMT-1536 (upifitamab rilsodotin) administered as an intravenous infusion once every four weeks. Patients with tumor types likely to express NaPi2b were enrolled in dose escalation. Patients with platinum-resistant ovarian cancer and non-small cell lung cancer (adenocarcinoma subtype) were enrolled in the expansion segment of this study. Patients with platinum-resistant, high-grade serous ovarian cancer were enrolled in the UPLIFT segment of this study. In addition to safety assessments, the pharmacokinetics of the drug were assessed along with ADC activity. A QTc sub-study was added for the UPLIFT cohort for a sub-set of sites.
Detailed description
This is a multi-center study of XMT-1536 (upifitamab rilsodotin) in patients with tumors likely to express NaPi2b, focusing on patients with platinum-resistant ovarian cancer and non-small cell lung cancer, adenocarcinoma subtype. XMT-1536 (upifitamab rilsodotin) was administered as an intravenous infusion once every four weeks. The study consisted of three segments: dose escalation (DES), dose expansion (EXP), and the pivotal cohort (UPLIFT). The DES segment studied small groups of patients who received increased doses. A Safety Review Committee was established to review the data from each dose level before moving to the next higher dose. The dose escalation cohort has ended and is no longer enrolling patients. Enrollment into the EXP segment consisted of 2 parallel cohorts of patients to confirm the dose that has been identified in DES and estimate the objective response rate in each patient population. The EXP and UPLIFT cohorts are no longer enrolling patients. All adverse events were graded according to the National Cancer Institute (NCI) Common Terminology Criteria version (CTCAE v5.0). Throughout the study, pharmacokinetics were measured using proprietary assays developed by Mersana. Anti-cancer activity were measured via RECIST.
Study design
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 5
- Model description
- Open-label, dose escalation to reach MTD. The MTD will be confirmed in parallel cohorts: patients with platinum-resistant ovarian cancer; patients with non-squamous NSCLC, adenocarcinoma subtype
| Arm | Type | Receives |
|---|---|---|
| Dose Escalation | Experimental | Drug: upifitamab rilsodotinXMT-1536 (upifitamab rilsodotin) treatment is administered in groups of patients who will receive doses that increase over time. This cohort is closed to enrollment. |
| Dose Expansion - Ovarian Cancer | Experimental | Drug: upifitamab rilsodotinOnce the maximum tolerated dose or recommended Phase 2 dose is achieved in dose escalation, new groups of patients will receive XMT-1536 (upifitamab rilsodotin) at this fixed-dose. This cohort is closed to enrollment. |
| Dose Expansion - NSCLC adenocarcinoma | Experimental | Drug: upifitamab rilsodotinOnce the maximum tolerated dose or recommended Phase 2 dose is achieved in dose escalation, new groups of patients will receive XMT-1536 (upifitamab rilsodotin) at this fixed-dose. This cohort is closed to enrollment. |
| Pivotal Cohort (UPLIFT) | Experimental | Drug: upifitamab rilsodotinPatients with platinum-resistant ovarian cancer will receive XMT-1536 (upifitamab rilsodotin) to further confirm the efficacy. This cohort is closed to enrollment. |
| QTc Sub-Study | Experimental | Drug: upifitamab rilsodotinFor sites participating in the sub-study, patients with platinum -resistant ovarian cancer will have the option to enroll in this sub-study to evaluate potential changes in the QTc interval following administration of XMT-1536. This cohort is closed to enrollment. |
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 |
|---|---|---|
| upifitamab rilsodotinAlso: XMT-1536, UpRiXMT-1536 will be administered once every 28 days until disease progression, unacceptable toxicity, or either the patient or study physician determines it is in the best interest of the patient to discontinue participation in the study. For sites participating in the sub-study, patients with platinum -resistant ovarian cancer will have the option to enroll in this sub-study to evaluate potential changes in the QTc interval following administration of XMT-1536 | Drug | Dose Escalation, Dose Expansion - NSCLC adenocarcinoma, Dose Expansion - Ovarian Cancer, Pivotal Cohort (UPLIFT), QTc Sub-Study |
Primary outcome
DES: Maximum tolerated dose or recommended Phase 2 dose
Time frame: Up to 36 weeks, from the date of first dose until unacceptable side effects or a dose-limiting toxicity is met
Evaluate adverse events and concomitant medication use after XMT-1536 (upifitamab rilsodotin) doses
DES and EXP: Safety and Tolerability
Time frame: First dose up until 30 days after study termination
Evaluate incidence and severity of adverse events
EXP: Anti-neoplastic effects of XMT-1536 (upifitamab rilsodotin)
Time frame: Every 6 weeks for up to 36 weeks
Monitor tumor size
UPLIFT: Investigator-assessed objective response rate (ORR) of XMT-1536 (upifitamab rilsodotin) in the ITT-Higher NaPi2b population
Time frame: Every 8 weeks until disease progression or up to 24 months
Confirmed ORR is defined as the proportion of patients who have achieved a confirmed complete response (CR) or partial response (PR) per RECIST v1.1 after the initiation of study treatment.
QTc Sub-study: Evaluation of the concentration response analysis of XMT-1536 versus the change in QTcF values
Time frame: 60 minutes prior to first dose, up to 26 hours after Cycle 3 dose
"The concentration-QTcf change from baseline deltaQTcF analysis and analysis of central tendency for deltaQTcF
11 secondary outcomes
DES and EXP: Time of maximum observed concentration of XMT-1536 (upifitamab rilsodotin)
Time frame: Daily for one week after first dose; weekly until 28 days after first dose; immediately before and after and 1 week after all subsequent doses
DES and EXP: Maximum concentration of XMT-1536 (upifitamab rilsodotin)
Time frame: Daily for one week after first dose; weekly until 28 days after first dose; immediately before and after and 1 week after all subsequent doses
DES and EXP: Area under the concentration curve of the last measurable concentration of XMT-1536 (upifitamab rilsodotin)
Time frame: Daily for one week after first dose; weekly until 28 days after first dose; immediately before and after and 1 week after all subsequent doses
DES: Anti-neoplastic effects of XMT-1536 (upifitamab rilsodotin)
Time frame: Every 6 weeks for up to 36 weeks
DES and EXP: Anti-drug antibody and neutralizing antibody
Time frame: Every 6 weeks for up to 36 weeks
UPLIFT: Confirmed Investigator-assessed objective response rate of XMT-1536 (upifitamab rilsodotin) regardless of NaPi2b expression
Time frame: Every 8 weeks until disease progression or up to 24 months
UPLIFT: Confirmed objective response rate by independent radiology review (IRR) for patients with high NaPi2b and overall
Time frame: Every 8 weeks until disease progression or up to 24 months
UPLIFT: Duration of objective response (DOR)
Time frame: 4 weeks after first response and every 8 weeks until disease progression or up to 24 months
UPLIFT: Incidence and severity of adverse events
Time frame: First dose up until 60 days after study termination
QTc Sub-Study: Evaluation of the effect of XMT-1536 on QTcF in patients with platinum-resistant HGSOC by timepoint analysis
Time frame: 60 minutes prior to first dose, up to 26 hours after Cycle 3 dose
QTc Sub-Study: Evaluation of the effect of XMT-1536 on the PR-interval (PR), QRS duration (QRS), Heart Rate (HR), and ECG morphology
Time frame: 60 minutes prior to first dose, up to 26 hours after Cycle 3 dose
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 13 Nov 2023.
- Individual participant dataSharing planned: No
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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.
Robert Burger, MD study director
Mersana Therapeutics
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 1/2 study testing upifitamab rilsodotin in people with Platinum Resistant Ovarian Cancer and Non Small Cell Lung Cancer Metastatic, run by Mersana Therapeutics at 1 site 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: under way, not looking for participants, as of the sponsor's last update on 13 Nov 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site 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 combined 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.
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
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?
DES: Maximum tolerated dose or recommended Phase 2 dose (time frame: Up to 36 weeks, from the date of first dose until unacceptable side effects or a dose-limiting toxicity is met). The study lists 5 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 13 Nov 2023.