Study of DP303c Administered Intravenously to Subjects With HER2-Positive in Advanced Solid Tumors

NCT04146610 | Unknown Phase 1

• 1 other identifier: DP303c201801
• Study Type: interventional
• Target: 30
• Locations: 1 country
• Sites: 1

Brief Summary

A phase Ia, multicenter, open and dose-increasing study of DP303c to evaluate the safety , pharmacokinetics, immunogenicity and antitumor activity of subjects with HER2-positive advanced solid tumors.

Conditions

Neoplasms

Outcome Measures

Primary Outcomes (1)

• Maximal Tolerance Dose (MTD) of Dp303c

  The dose level in which \>= 2 out of 6 patients have dose-limiting toxicity (DLT). The MTD is defined as the previous dose level.

  The first treatment cycle 21 days

Secondary Outcomes (6)

• Maximum concentration (Cmax) of DP303c

  approximately 2 years

• Time of peak plasma concentration (Tmax)

  approximately 2 years

• Area under the plasma concentration time curve (AUC) of DP303c

  approximately 2 years

• Overall response rate (ORR)

  approximately 2 years

• Duration of Response (DoR)

  approximately 2 years

Study Arms (1)

Dp303c

EXPERIMENTAL

Multiple dose grouping

Drug: an antibody drug conjugate

Interventions

an antibody drug conjugate DRUG

Multiple dose grouping

Also known as: ADC

Dp303c

Eligibility Criteria

• Age: 18 Years - 75 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Voluntary agreement to provide written informed consent；
• Aged 18 to 75 years, both male and female;
• Patients with advanced solid tumors diagnosed by histology and / or cytology, confirmed to be HER2 positive by pathological examination, unable to accept or have no standard treatment, failure of standard treatment (disease progress or treatment without remission after treatment) or intolerable patients; HER2-positive is defined as IHC 2+ and ISH positive or IHC 3+； IHC scores of breast cancer and gastric cancer are based on their respective standards, while IHC scores of other cancers are based on the scoring standards of breast cancer；
• The ECOG performance status is 0 to 1,and the expected survival time is more than 3 months；
• Subjects must have laboratory values within the limits described below:
• ANC ≥1.5 x 109/L Platelet count ≥100 x 109/L Hemoglobin ≥9 g/dL Serum creatinine within normal limits OR creatinine clearance ≥60 mL/minute Serum total bilirubin ≤1.5 x ULN (up to 3 x ULN in subjects with Gilbert's syndrome) AST (SGOT) and ALT (SGPT) ≤2.5 x ULN (OR ≤5 X ULN for subjects with liver metastases) PT/INR and APTT ≤1.5 x ULN
• According to the RECIST v1.1 standard, there must be a measurable lesion at the base line；
• WOCBP must have a negative pregnancy test prior to study entry；
• WOCBP and male subjects must agree to use adequate contraception from study entry through at least 12 weeks after the last dose of study drug (see Appendix 5)；
• A washout period is required for subjects who have recently received systemic antitumor therapy. The period prior to the subject's planned first dose of DP303c must be either at least 28 days or 5 half-lives, whichever is shorter. Antitumor therapy includes chemotherapy, immunotherapy, targeted therapy, endocrine therapy, radiotherapy (except local radiotherapy for pain relief, 14 days after treatment).

You may not qualify if:

• Pregnant or breastfeeding women；
• Not recovered from AEs caused by previous drugs or radiotherapy (reference NCI CTCAE 5.0, ≤Grade 1 or at baseline), with the exception of alopecia；
• History of cardiac dysfunction with LVEF \<40% while on trastuzumab therapy；
• Subjects with a history of allergy to any components(tratozumab analogues, MMAE, sodium citrate dihydrate, citrate monohydrate, polysorbitol 20 and sucrose, etc.) of DP303cand those who researchers consider to be more serious；
• A history of central nervous system (CNS) metastases or epilepsy, asymptomatic or stable, and not requiring treatment at least 4 weeks before study therapy began；
• Active lung infection or pneumonitis or a history of non-infectious interstitial lung disease；
• Requires supplemental oxygen；
• History of congestive heart failure, unstable angina pectoris, unstable atrial fibrillation, or cardiac arrhythmia. Subjects who have the following types of cardiac impairment at the time of enrollment:
• New York Heart Association class III or IV heart disease Uncontrolled angina, congestive heart failure, or myocardial infarction within 6 months prior to enrolment An LVEF by echocardiogram (ECHO) or multi-gated acquisition (MUGA) scan \<50% or below the lower limit of normal for the institution QT interval prolongation (\>450 ms in males, \>470 ms in females),QT interval correction (QTcF) was corrected by Fridericia formula
• In the first 90 daysof the study, Cumulative anthracycline dose ≥360 mg/m2 doxorubicin or equivalent；
• Peripheral neuropathy ≥Grade 2 or greater (NCI CTCAE v 5.0)；
• Non-manageable electrolyte imbalances including hypokalemia, hypocalcemia, or hypomagnesemia (≥Grade 2 or greater based on NCI CTCAE v 5.0)；
• Any uncontrollable intercurrent illness, infection, or other conditions that could limit study compliance or interfere with assessments；
• Serologic status reflecting active hepatitis B or C infection；
• Subjects with immunodeficiency, including HIV positive；

Sponsors & Collaborators

• CSPC ZhongQi Pharmaceutical Technology Co., Ltd.: lead

Study Sites (1)

Fudan University Cancer Hospital

Shanghai, China

Location

Related Publications (1)

• Zhang J, Du Y, Meng Y, Liu X, Mu Y, Liu Y, Shi Y, Wang J, Zang A, Gu S, Liu T, Zhou H, Guo H, Xiang S, Zhang X, Wu S, Qi H, Li M, Hu X. First-in-human study of DP303c, a HER2-targeted antibody-drug conjugate in patients with HER2 positive solid tumors. NPJ Precis Oncol. 2024 Sep 12;8(1):200. doi: 10.1038/s41698-024-00687-7.

  PMID: 39266619 DERIVED

MeSH Terms

Conditions

Neoplasms

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: October 28, 2019
• First Posted: October 31, 2019
• Study Start: November 1, 2019
• Primary Completion: June 1, 2021
• Study Completion: June 1, 2021
• Last Updated: October 31, 2019

Record last verified: 2019-10

Data Sharing

• IPD Sharing: Will not share

Locations

CN (1)