A Study of AZD6750 for Advanced Solid Tumors

This study is looking into the safety of a drug called AZD6750, which is an immunotherapy. It's for adults with certain advanced or metastatic (spread to other parts of the body) solid tumors, including melanoma, non-small cell lung cancer, skin squamous cell carcinoma, renal cell carcinoma (kidney cancer), and Merkel cell carcinoma. Some participants will receive AZD6750 alone, while others may receive it in combination with rilvegostomig, another immunotherapy drug. Researchers will also look at how well these treatments work. To join, you need to be at least 18 years old, have a good general health status (ECOG PS of 0 to 1), and have a tumor sample available for testing. Your body weight must be at least 35 kg, and you need to have adequate organ function. The study plans to enroll about 60 participants.

Study design
This is an open-label study, meaning both you and your doctors will know which treatment you are receiving. It is a Phase I/II study, which means it will first look at safety and then at how well the treatment works, and plans to enroll about 60 participants.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Your safety will be monitored from the start of the study until 90 days after your last dose. If you are in the part of the study looking at how well the treatment works, your progress will be measured every 6 weeks for 48 weeks, and then every 12 weeks until your disease progresses or you pass away, which is expected to be about 2 years.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07115043

A Study to Investigate Safety of AZD6750 in Adult Participants With Select Advanced or Metastatic Solid Tumors

Recruiting
PHASE1Ages 18+InterventionalTreatment
AstraZeneca
~120 participants
Updated 2026-08-19 on ClinicalTrials.gov
What's tested:AZD6750rilvegostomig

At a glance

Recruiting sites
12 of 13 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Safety- Part 1A & Part 2A (dose escalation) and Part 2B (dose expansion)
Measured over Measured from the informed consent until Day 90 post-last dose.
+1 more outcome measured
Melanoma
Non-small Cell Lung Cancer
Squamous Cell Carcinoma (Skin)
Renal Cell Carcinoma
Merkel Cell Carcinoma
Triple Negative Breast Cancer
Head and Neck Squamous Cell Carcinoma
Gastric Cancer/Gastroesophageal Junction Cancer
High Grade Serous Ovarian Carcinoma
13 sites across 8 states
South Korea4
Texas2
Japan2
Michigan1
Missouri1
Pennsylvania1
Virginia1
Australia1
AstraZeneca Clinical Study Information Center
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Do you actually qualify for this trial?

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Eligibility criteria

Inclusion

Participant ≥ 18 year
ECOG PS of 0 to 1
Provision of 'archival' tumor specimen
At least one measurable lesion according to RECIST v1.1,
Minimum life expectancy of 12 weeks
Adequate and stable cardiac function
Adequate bone marrow, liver and kidney function
Body weight ≥ 35 kg
Capable of giving signed informed consent
Participants with Stage IV NSCLC Dose Escalation/Backfills

Exclusion

Any evidence of:
History or planned organ or allogeneic stem cell transplantation.
Active or prior documented autoimmune or inflammatory disorders, within the past 3 years
Any prior toxicities that led to permanent discontinuation of prior immunotherapy
Persistent toxicities (CTCAE Grade ≥ 2) caused by previous anti-cancer therapy
Brain metastases unless treated, asymptomatic, stable, and not requiring continuous corticosteroids
Acute untreated or symptomatic malignant spinal cord compression, or a history of leptomeningeal carcinomatosis.
Active uncontrolled or chronic infection of hepatitis B, hepatitis C
Prior history of Grade ≥ 3 non-infectious pneumonitis.
Participant requires chronic immunosuppressive therapy (including steroids \> 10 mg prednisone/day or equivalent).
Receipt of live attenuated vaccine within 30 days.
Previous treatment with anti-TIGIT therapy
1L NSCLC participants with genetic alteration such as EGFR that has a targeted therapy in 1L as per local SoC
  • Safety- Part 1A & Part 2A (dose escalation) and Part 2B (dose expansion)Measured from the informed consent until Day 90 post-last dose.

    To assess the safety and tolerability, characterize the DLTs, and determine the MTD and RP2D(s) of AZD6750 as a single agent and in combination with other anti-cancer agents as specified in each respective module

  • Efficacy- Part 2B only (dose expansion)Measured every 6 weeks for 48 weeks and every 12 weeks thereafter from first dose until disease progression or death in the absence of disease progression(approximately 2 years)

    To assess the preliminary anti-tumor activity of AZD6750 in combination with other anti-cancer agents.