At a glance
- What the study gets you
- Access to the study treatment being tested
- Type of study
- Interventional (receives a drug or procedure)
- Time in hospital
- In-person visits at study sites — visit count not specified by the sponsor
- Drug or intervention
- IAM1363 (drug)
- How long the study runs
- Study runs about 57 months (dates as stated)
- About the drug or intervention
- IAM1363 — drug: IAM1363 monotherapy OR IAM1363 in combination with capecitabine + trastuzumab OR IAM1363 in combination with capecitabine + zanidatamab OR IAM1363 in combination with T-Dxd OR IAM1363 in combination with pembrolizumab +/- carboplatin and pemetrexed
- Patient visit burden
- Not specified by the sponsor
- Type of study
- Testing a treatment
- Ages
- 18 Years and over
- Who
- All
- Number of participants
- 383
- Started
- 2024-03-25
- Last checked
- 2026-09
Plain English Summary
What is this study?
- • Testing a new treatment for her2 mutation-related tumors
- • Phase1 - 383 participants
- • This is a Phase 1/1b open-label, multi-center dose escalation and dose optimization study designed to evaluate the safety and preliminary efficacy of IAM1363 in participants with advanced cancers that harbor HER2 alterations
Who can take part?
- • Ages 18 Years and over
- • Diagnosed with her2 mutation-related tumors
Where?
- • Chelsea - Royal Marsden NHS Foundation Trust, Royal Marsden Hospital (RMH)/Chelsea)
- • Oxford - Oxford University Hospitals NHS Foundation Trust Churchill Hospital
- • Sutton - Royal Marsden NHS Foundation Trust, Royal Marsden Hospital (RMH)/Sutton
This is a simplified summary. Always discuss with your doctor before making any decisions.
About This Trial
This is a Phase 1/1b open-label, multi-center dose escalation and dose optimization study designed to evaluate the safety and preliminary efficacy of IAM1363 in participants with advanced cancers that harbor HER2 alterations.
More detail
This is a Phase 1/1b open-label, multi-center study, designed to evaluate IAM1363 in participants with advanced cancers that harbor HER2 alterations. This study consists of the following 4 parts: * Part 1 (Monotherapy Dose Escalation) * Part 2 (Dose Optimization) * Part 3 (Dose Expansion) * Part 4 (Combination Cohorts) Part 1 will enroll participants with a confirmed, relapsed/refractory malignancy with documented diagnosis of HER2 alterations including participants with brain metastases. Once a provisional maximum tolerated dose (MTD)/recommended Phase 2 dose (RP2D) has been determined, Part 2 will enroll additional cohorts to optimize dose selection and to further evaluate the safety and preliminary efficacy of IAM1363. Following completion of Dose Optimization, Part 3 will be opened to enroll tumor-specific cohorts utilizing a Simon 2-Stage Minimax Design to evaluate IAM1363 at the selected dose(s). Part 4 will enroll 4 cohorts of participants who will receive IAM1363 in combination with other anti-cancer agents.
How this trial compares with your answers
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What we know so far
Still need:
- • Tell us your age for better matching
- • Tell us your sex for better matching
Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.
Eligibility at a Glance
Key info
- Age: 18 Years and over
- Who can join: All genders
Biomarkers mentioned
What the study is looking for
- ✓Age ≥ 18 years
- ✓Have relapsed/refractory HER2-altered cancer; for selected cohorts, prospective confirmation of HER2 alteration...
- ✓Have progression of disease after the last treatment that goes through your whole body, or be intolerant of last treatment that goes through your whole body
- ✓Have radiographically cancer that can be measured on scans by (standard scan measurements) and/or RANO-BM
- ✓activity scale (ECOG) performance score 0-1
Who cannot take part
- ✗Clinically significant heart disease
- ✗Infection with human immunodeficiency virus (HIV)-1 or HIV-2. Exception: Participants with well-controlled HIV...
- ✗Current active liver disease including hepatitis A, hepatitis B , or hepatitis C
- ✗Refractory nausea and vomiting, malabsorption, external biliary shunt, or significant small bowel resection that...
- ✗Uncontrolled diabetes
See the full criteria
Where Is This Study? (3 UK sites)
Royal Marsden NHS Foundation Trust, Royal Marsden Hospital (RMH)/Chelsea)
Chelsea SW3 6JJ, United Kingdom
Oxford University Hospitals NHS Foundation Trust Churchill Hospital
Oxford OX3 7LE, United Kingdom
Royal Marsden NHS Foundation Trust, Royal Marsden Hospital (RMH)/Sutton
Sutton SM2 5PT, United Kingdom
How to Get in Touch
Iambic Therapeutics, Inc., Senior Medical Director
Sponsor contactCONTACT
