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AZD6750

Phase 1

Melanoma | Small molecule | Oncology |AstraZeneca PLC|Last Updated: Aug 19, 2026

Success Probability

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Market & Valuation

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Trial Design

CONTROLLED
Total Trials1
Total Enrollment120

FDA Designations

No designations recorded

Clinical trial landscape

AZD6750 · 1 trial · 9 indications

Phase 1 1
NCT07115043A Study to Investigate Safety of AZD6750 in Adult Participants With Select Advanced or Metastatic Solid TumorsMelanoma
RECRUITING120 Analytics
PHASE1RECRUITING
A Study to Investigate Safety of AZD6750 in Adult Participants With Select Advanced or Metastatic Solid Tumors
MelanomaUnlock trial analytics

Study Endpoints

Primary Endpoints

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.

Secondary Endpoints

Pharmacodynamic- Part 1A & Part 2A (dose escalation) and Part B (dose expansion)
Measured with baseline and On-treatment biopsy. On-treatment biopsy is planned during Cycle 2 during Cycle 2 (each cycle is 28 days or 21 days depending on Module/dosing schedule)
Immunogenicity- Part 1A & 2A (dose escalation) and Part 2B (dose expansion)
Measured from pre-infusion on Cycle 1 up to Day 28 post last dose. Each cycle is 28 days or 21 days depending on Module/dosing schedule).
Efficacy (Part 1A and 2A)
Measured every 6 weeks for 48 weeks and every 12 weeks thereafter thereafter from first dose until disease progression or death in the absence of disease progression (approximately 2 years)
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Study Design & Arms

AllocationNON_RANDOMIZED
MaskingNONE
ModelPARALLEL
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
Module 1EXPERIMENTALAZD6750 administered intravenously (IV) as a single agent
Module 2EXPERIMENTALAZD6750 given in combination with rilvegostomig (IV)

Interventions

NameTypeDescription
AZD6750DRUGAZD6750- CD8 guided IL-2
rilvegostomigDRUGRilvegostomig- PD1-TIGIT bispecific antibody
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Eligibility Criteria

Age Range18 Years to N/A
SexALL
Healthy VolunteersNo
Study Sites13

Inclusion criteria: * 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 w...

Countries:United StatesAustraliaJapanSouth Korea
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Recent Changes (Last 90 Days)

LOWAug 20, 2026NCT07115043Enrollment: 60 → 120
LOWAug 20, 2026NCT07115043Enrollment: 60 → 120
LOWAug 20, 2026NCT07115043Enrollment: 60 → 120
LOWAug 20, 2026NCT07115043Enrollment: 60 → 120
LOWJul 7, 2026NCT07115043lastUpdatePostDate: changed
LOWJul 7, 2026NCT07115043lastUpdatePostDate: changed
LOWJun 11, 2026NCT07115043lastUpdatePostDate: changed
LOWJun 11, 2026NCT07115043lastUpdatePostDate: changed

Frequently asked questions about AZD6750

What is AZD6750 used for?

AZD6750 is an investigational small molecule being developed for the treatment of melanoma and other advanced or metastatic solid tumors. It is currently being studied in adult participants with conditions including non-small cell lung cancer, squamous cell carcinoma of the skin, renal cell carcinoma, Merkel cell carcinoma, triple negative breast cancer, head and neck squamous cell carcinoma, gastric cancer, and high grade serous ovarian carcinoma.

Who makes AZD6750?

AZD6750 is being developed by AstraZeneca PLC, a biopharmaceutical company traded on the stock exchange under the ticker symbol AZN. The company is currently conducting clinical research on this investigational drug candidate.

What phase is AZD6750 in?

AZD6750 is in Phase 1 clinical development. It is an investigational drug that has not been approved by regulatory authorities. The drug is currently being evaluated in an early-stage clinical trial to assess its safety in adult participants with select advanced or metastatic solid tumors.

What clinical trials is AZD6750 in?

AZD6750 is being studied in a Phase 1 clinical trial with the identifier NCT07115043. This trial is titled 'A Study to Investigate Safety of AZD6750 in Adult Participants With Select Advanced or Metastatic Solid Tumors' and is currently recruiting participants in the United States, Australia, Japan, and South Korea.

How does AZD6750 work?

AZD6750 is a small molecule therapeutic agent. The specific molecular target of AZD6750 has not been disclosed in available information. The drug is being investigated for its potential to treat various types of cancer, including melanoma and other solid tumors.