First-line Therapy

8

Review clinical trials related to First-line Therapy. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Zanidatamab in Combination With Pembrolizumab and Chemotherapy in HER2 and PD-L1 Positive Metastatic Gastroesophageal Adenocarcinoma (GEA) Patients

The ZANGEA trial is a open-label, single arm, multicenter phase II trial assessing the efficacy of zanidatamab in combination with pembrolizumab and chemotherapy in patients with metastatic gastroesophageal adenocarcinoma (GEA). The patients need to be previously untreated in the palliative setting and tested positive for HER2 and PD-L1.

Participants needed: 80
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Institut für Klinische Krebsforschung IKF GmbH at Krankenhaus NordwestUpdated: Jun 30, 2026Locations: 20
Eligibility criteria

Patient* has signed and dated a written informed consent form in accordance with... [+14]

Patient has any known contraindication including allergy or hypersensitivity to... [+17]

Status: Not yet recruiting

Creating Opportunities For Personal Empowerment (COPE) In Women With Breast Cancer During First-Line Therapy: A Pilot Randomized Controlled Trial

To learn if the Creating Opportunities for Personal Empowerment (COPE) intervention is feasible, acceptable, and helpful (compared to usual care) in women with breast cancer who are receiving first line treatment.

Participants needed: 40
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: M.D. Anderson Cancer CenterUpdated: May 28, 2026Locations: 1
Eligibility criteria

Female [+7]

Diagnosed with multiple tumor types [+3]

Status: Recruiting

A Multicenter RCT of "3+7" vs Venetoclax + CACAG in Newly Diagnosed Mid/High-Risk AML Patients

The purpose of this study is to compare the efficacy and safety of venetoclax combined with the CACAG regimen with the traditional "3+7" regimen in the treatment of newly diagnosed intermediate- or high-risk acute myeloid leukemia (AML).

Participants needed: 160
Trial details
Phase: Phase 2Age: 14-75Biological sex: AllType: InterventionalSponsor: Chinese PLA General HospitalUpdated: May 8, 2026Locations: 1
Eligibility criteria

Not listed

Status: Not yet recruiting

Efficacy and Safety of QL1706 Combined With Nab-paclitaxel and Cisplatin as 1st Line Therapy for Advanced or Metastatic Esophageal Squamous Cell Carcinoma

The purpose of this study is to assess the efficacy and safety of QL1706 combined with nab-paclitaxel and cisplatin in first-line therapy for patients with advanced or metastatic esophageal squamous cell carcinoma. QL1706 is a anti-PD-1 and anti-CTLA4 antibody.

Participants needed: 50
Trial details
Phase: Phase 2Age: 18-75Biological sex: AllType: InterventionalSponsor: The First Affiliated Hospital of Henan University of Science and TechnologyUpdated: Apr 16, 2026
Eligibility criteria

Subjects participate voluntarily and sign informed consent. [+8]

Have received anti-PD-1 or anti-PD-L1 antibody therapy; [+15]

Status: Recruiting

Fruquintinib Combined With Trastuzumab and XELOX as First-line Treatment in Patients With HER2-positive Advanced Gastric Cancer

This study was designed to evaluate the safety and efficacy of fruquintinib plus trastuzumab, and XELOX as first-line treatment for HER2-positive advanced gastric or gastroesophageal junction (GEJ) adenocarcinoma.

Participants needed: 45
Trial details
Phase: Phase 1, Phase 2Age: 18-75Biological sex: AllType: InterventionalSponsor: Henan Cancer HospitalUpdated: Jan 12, 2026Locations: 1
Eligibility criteria

Have fully understood the study and voluntarily signed the informed consent; [+16]

Failure to comply with the study protocol or study procedure; [+25]

Status: Not yet recruiting

Trastuzumab Rezetecan Combined With Pertuzumab and Iparomlimab and Tuvonralimab for Biliary Tract Cancer

Based on unmet clinical needs, relevant research backgrounds, and scientific evidence, it is planned to conduct a prospective, dual-cohort exploratory study. The aim of this study is to explore the efficacy and safety of ricartuzumab combined with pertuzumab and epalrestat-vorolizumab in the first-line treatment of HER2-expressing locally advanced or metastatic biliary tract cancer. It is expected to provide more treatment options for biliary tract cancer patients, optimize treatment strategies, and improve patients' long-term survival rates.

Participants needed: 63
Trial details
Phase: Phase 2Age: 18-75Biological sex: AllType: InterventionalSponsor: Union Hospital, Tongji Medical College, Huazhong University of Science and TechnologyUpdated: Aug 19, 2025
Eligibility criteria

Patients must voluntarily participate in the trial, provide fully informed conse... [+12]

Histologically or cytologically confirmed ampullary carcinoma, small cell carcin... [+18]

Status: Recruiting

Low Dose Nivolumab With Chemotherapy vs Standard Chemotherapy as First-Line Treatment in Advanced or Metastatic NSCLC

This is a multicenter, two-arm randomized, parallel group design trial to evaluate superiority and safety of low dose Nivolumab (40mg) combined with standard chemotherapy versus standard chemotherapy alone in patients with non-small cell lung cancer.

Participants needed: 123
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Dr Arvindran A/L AlagaUpdated: Jul 3, 2025Locations: 1
Eligibility criteria

Male/female participants who are at least 18 years of age on the day of signing... [+10]

Presence of EGFR, ALK , ROS1 mutation(s). [+11]

Status: Not yet recruiting

Fruquintinib Combined With PD-1 Inhibitor as First-line Maintenance Therapy for Advanced Gastric Cancer

This study was designed to explore the efficacy and safety of fruquintinib combined with PD-1 inhibitors as first-line maintenance therapy for advanced HER-2 Negative Gastric Cancer.

Participants needed: 55
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Ruijin HospitalUpdated: Mar 21, 2025Locations: 1
Eligibility criteria

Voluntarily signed the informed consent and had good compliance; [+6]

Participated in other drug clinical trials within 4 weeks before enrollment; [+23]