Trial Title:
A Study of DB-1311 in Advanced/Metastatic Solid Tumors
NCT ID:
NCT05914116
Condition:
Advanced Solid Tumors
Conditions: Official terms:
Neoplasms
Conditions: Keywords:
B7-H3
SCLC
NSCLC
ESCC
CRPC
Melanoma
small cell lung cancer
non-small cell lung cancer
esophageal squamous cell carcinoma
castration-resistant prostate cancer
Study type:
Interventional
Study phase:
Phase 1/Phase 2
Overall status:
Recruiting
Study design:
Allocation:
Non-Randomized
Intervention model:
Sequential Assignment
Primary purpose:
Treatment
Masking:
None (Open Label)
Intervention:
Intervention type:
Drug
Intervention name:
DB-1311
Description:
Administered I.V.
Arm group label:
DB-1311 Dose Expansion 1
Arm group label:
DB-1311 Dose Expansion 2
Arm group label:
DB-1311 Dose Expansion 3
Arm group label:
DB-1311 Dose Expansion 4
Arm group label:
DB-1311 Dose Expansion 5
Arm group label:
DB-1311 Dose Expansion 6
Arm group label:
DB-1311 Dose Level 1
Arm group label:
DB-1311 Dose Level 2
Arm group label:
DB-1311 Dose Level 3
Arm group label:
DB-1311 Dose Level 4
Arm group label:
DB-1311 Dose Level 5
Summary:
This is a dose-escalation and dose-expansion Phase 1/2a trial to evaluate the safety and
tolerability of DB-1311 in subjects with advanced solid tumors.
Detailed description:
This is a multicenter, open-label, multiple-dose, FIH Phase 1/2a study. Phase 1 adopts an
accelerated titration at first dose level followed with classic "3+3" design to identify
the MTD and/or RP2D. Phase 2a is a dose expansion phase to confirm the safety,
tolerability and explore efficacy in selected malignant solid tumors treated with DB-1311
as monotherapy.
Criteria for eligibility:
Criteria:
Inclusion Criteria:
1. Male or female adults (defined as ≥ 18 years of age or acceptable age according to
local regulations at the time of voluntarily signing of informed consent).
2. Histologically or cytologically confirmed unresectable advanced/metastatic solid
tumor that has relapsed or progressed on or after standard systemic treatments, or
is intolerable with standard treatment; or for which no standard treatment is
available.
3. At least one measurable lesion as assessed by the investigator according to response
evaluation criteria in solid tumors (RECIST) version 1.1 criteria.
Castrate-resistant prostate cancer (CRPC) participants with bone only disease may be
eligible on a case-by- case basis after discussion with the Medical Monitor.
4. Has a life expectancy of ≥ 3 months.
5. Has an Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0-1.
6. Has LVEF ≥ 50% by either echocardiography (ECHO) or multiple-gated acquisition
(MUGA) within 28 days before enrollment.
7. Is willing to provide pre-existing resected tumor samples or undergo fresh tumor
biopsy for the measurement of B7-H3 level and other biomarkers if no
contraindication.
Note: there is no minimum B7-H3 expression level mandatory for entry into the study.
8. Is capable of comprehending study procedures and risks outlined in the informed
consent and able to provide written consent and agree to comply with the
requirements of the study and the schedule of assessments.
9. Male and female subjects of reproductive/childbearing potential must agree to use
adequate contraceptive methods (e.g., double barrier or intrauterine contraceptive)
during the study and for at least 4 months and 7 months after the last dose of study
drug, respectively.
10. Male subjects must not freeze or donate sperm starting at screening and throughout
the study period, and at least 4 months after the final study drug administration.
11. Female subjects must not donate, or retrieve for their own use, ova from the time of
screening and throughout the study treatment period, and for at least 7 months after
the final study drug administration.
12. SCLC participants (Phase 2a Cohort 1 ONLY):
- Pathologically documented locally advanced, or metastatic SCLC not amenable to
curative surgery or radiation.
- Relapsed/progressed on or after 2 cycles of platinum-based chemotherapy in
combination with/without anti-PD-1/anti-PD-L1 monoclonal antibody or intolerant
to completion of 2 cycles of platinum-based chemotherapy due to the toxicity
for locally advanced or metastatic disease.
13. NSCLC participants (Phase 2a Cohort 2 ONLY):
- Pathologically documented locally advanced, or metastatic NSCLC and is not
amenable to curative surgery or radiation.
- Has received prior treatment with platinum-based chemotherapy regimen and/or
anti-PD-1/PD-L1 antibody-based regimen in the advanced/unresectable, or
metastatic setting unless unable or unwilling. Participants with NSCLC known to
harbor a genomic alteration(s) other than EGFR mutation(s) (e.g., ALK
rearrangement, ROS1 rearrangement, KRAS G12C mutation, BRAF V600E mutation,
NTRK1/2/3 Gene fusion, MET Exon 14 skipping, RET rearrangement etc.) for which
treatment is available must have also received prior treatment with at least 1
genotype-directed therapy.
14. ESCC participants (Phase 2a Cohort 3 ONLY):
- Pathologically documented locally advanced, or metastatic ESCC and is not
amenable to curative surgery or radiation.
- Having received at least one prior therapy for unresectable disease. Patients
with recurrence within 6 months of completion of neoadjuvant or adjuvant
therapy will be considered as having received one prior therapy for
unresectable disease.
15. CRPC participants (Phase 2a Cohort 4 ONLY):
- Pathologically documented metastatic adenocarcinoma of the prostate cancer.
- Progressive metastatic CRPC as defined: 1) castrate levels of serum
testosterone < 50 ng/dL AND 2) progressive disease as defined by PCWG3
criteria.
- Having received prior docetaxel (before or after an AR-targeted therapy).
Docetaxel rechallenge was allowed.
- Having received prior novel hormone therapy.
16. Melanoma participants (Phase 2a Cohort 5 ONLY)
• Histologically or cytologically confirmed diagnosis of unresectable Stage III or
metastatic melanoma not amenable to local therapy, must have had either:
- Previously treated with a PD-1 or PD-L1 inhibitor.
- If participants with BRAF gene mutant melanoma, must have had a prior treatment
regimen that included vemurafenib, dabrafenib, or another BRAF gene and/or
mitogen-activated protein kinase (MEK) protein inhibitor.
17. Participants with other solid tumors (Phase 2a Cohort 6 ONLY)
- Histologically or cytologically confirmed solid tumors.
- Progressed or relapsed after at least one prior standard therapeutic regimen
(Patients who have not received all approved or standard treatments for their
cancer must be informed that these alternatives to receiving DB-1311 are
available prior to consenting to participate in this trial).
Exclusion Criteria:
Unless otherwise specified, the exclusion criteria are common to both Phase 1 and Phase
2a. Subjects who meet any of the following criteria will be excluded from the study:
1. Prior treatment with B7-H3 targeted therapy.
2. Prior treatment with antibody drug conjugate with topoisomerase inhibitor (e.g.,
trastuzumab deruxtecan).
3. Has a medical history of symptomatic congestive heart failure (CHF) (New York Heart
Association [NYHA] classes II-IV) or serious cardiac arrhythmia requiring treatment.
4. Has a medical history of myocardial infarction or unstable angina within 6 months
before enrollment.
5. Has an average of Fredericia's formula-QT corrected interval (QTcF) prolongation to
> 470 millisecond (ms) in males and females based on a 12-lead electrocardiogram
(ECG) in triplicate.
6. Unable or unwilling to discontinue concomitant drugs that are known to prolong the
QT interval.
7. Has a medical history of interstitial lung diseases (e.g., non-infectious
interstitial pneumonia, pneumonitis, pulmonary fibrosis, and severe radiation
pneumonitis) or current interstitial lung diseases or who are suspected to have
these diseases by imaging at screening.
8. Has a history of underlying pulmonary disorder including, but not limited to,
pulmonary emboli within 3 months of the start of study treatment, severe asthma,
severe COPD, restrictive lung disease, and other clinically significant pulmonary
compromise or requirement for supplemental oxygen.
9. Any autoimmune, connective tissue or inflammatory disorders (e.g., rheumatoid
arthritis, Sjögren's, sarcoidosis) where there is documented, or a suspicion of
pulmonary involvement at the time of screening.
10. Has an uncontrolled infection requiring intravenous injection of antibiotics,
antivirals, or antifungals.
11. Know human immunodeficiency virus (HIV) infection.
12. Subjects have active viral (any etiology) hepatitis are excluded. However, subjects
with serologic evidence of chronic hepatitis B virus (HBV) infection (defined by a
positive hepatitis B surface antigen [HBsAg] test or a positive hepatitis B core
antibody test) who have a viral load below the limit quantification (HBV DNA titer <
1000 cps/mL or 200 IU/mL) and are not currently on viral suppressive therapy may be
eligible and should be discussed with the Sponsor's Medical Monitor. However,
subjects with a history of hepatitis C virus (HCV) infection who have completed
curative antiviral treatment and have a viral load below the limit of quantification
are eligible for study entry.
13. Is a lactating mother (women who are willing to temporarily interrupt breastfeeding
will also be excluded), or pregnant as confirmed by pregnancy tests performed within
7 days prior to enrollment.
14. Has spinal cord compression or clinically active central nervous system metastases,
defined as untreated and symptomatic, or requiring therapy with corticosteroids or
anticonvulsants to control associated symptoms. Subjects with clinically inactive
brain metastases may be included in the study. Subjects with treated brain
metastases that are no longer symptomatic and who require no treatment with
corticosteroids or anticonvulsants may be included in the study if they have
recovered from the acute toxic effect of radiotherapy. A minimum of 2 weeks must
have elapsed between the end of whole brain radiotherapy and study randomization.
15. Has unresolved toxicities from previous anticancer therapy, defined as toxicities
(other than alopecia) not yet resolved to NCI-CTCAE version 5.0, grade ≤ 1 or
baseline. Subjects with chronic Grade 2 toxicities (e.g., Grade 2 neuropathy) may be
eligible based on the discussion and agreement between Investigator and Sponsor.
16. Has multiple primary malignancies within 3 years before enrollment, except
adequately resected non-melanoma skin cancer (e.g., resected basal or squamous cell
skin cancer), curatively treated in-situ disease (e.g., carcinoma in situ of the
cervix or breast), other solid tumors curatively treated (e.g., superficial bladder
cancer), or contralateral breast cancer.
17. Has substance abuse or any other medical conditions that would increase the safety
risk to the subject or interfere with participation or evaluation of the clinical
study in the opinion of the investigator.
18. Has known hypersensitivity to either the drug substances or inactive ingredients in
the drug product.
19. Patients with other reasons that, in the opinion of the Investigator, make them
unsuitable to participate in this study.
Gender:
All
Minimum age:
18 Years
Maximum age:
N/A
Healthy volunteers:
No
Locations:
Facility:
Name:
BRCR Medical Center Inc.
Address:
City:
Plantation
Zip:
33322
Country:
United States
Status:
Not yet recruiting
Contact:
Last name:
H Amin
Facility:
Name:
Site 102
Address:
City:
Fairfax
Zip:
22031
Country:
United States
Status:
Not yet recruiting
Contact:
Last name:
Alexander Spira, MD, PhD, FACP
Facility:
Name:
Site 201
Address:
City:
Sydney
Zip:
2031
Country:
Australia
Status:
Recruiting
Contact:
Last name:
Charlotte Lemech, Dr.
Facility:
Name:
Site 202
Address:
City:
Nedlands
Zip:
6009
Country:
Australia
Status:
Not yet recruiting
Contact:
Last name:
Afaf Abed, Dr
Start date:
September 5, 2023
Completion date:
April 2025
Lead sponsor:
Agency:
DualityBio Inc.
Agency class:
Industry
Source:
DualityBio Inc.
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT05914116
