A Study of ATTR-01 in Participants With Select Epithelial Solid Tumours
Recruiting
Phase 1Phase 2Interventional Study
Solid Tumor, Adult
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 1/2
Study type
Interventional
Purpose
Treatment
Participants needed
72 (estimated)
Sponsor
Accession Therapeutics Limited · Industry
Who this trial is looking for
This trial is looking for adults with specific solid tumors. Participants will receive a new treatment designed to help their immune system fight the cancer.
Are You a Good Fit for This Trial?
You may be able to join if
I am at least 18 years old.
I have a solid epithelial tumor that often shows a certain marker.
I have received standard cancer treatments that didn't work for me.
My tumor has not been treated with radiation.
I have measurable cancer as defined by specific criteria.
I am in good enough health to participate.
I expect to live more than three months.
I am willing to follow hygiene measures to prevent virus spread.
You may not be able to join if
I have a severe fibrotic disease or autoimmune disease.
I have had serious side effects from PD-1 or PD-L1 therapies before.
I have any other serious health conditions that disqualify me.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
ATTR-01 is the experimental drug being studied in the ATTEST clinical trial. The drug is made from a common cold virus that has been changed to only infect and multiply in cancer cells. This virus delivers an immune therapy drug into the cancer that is intended to promote a participant's own immune system to attack the cancer. The first part of this trial (sub-protocol A) is a phase 1 trial includ…
ATTR-01 is the experimental drug being studied in the ATTEST clinical trial. The drug is made from a common cold virus that has been changed to only infect and multiply in cancer cells. This virus delivers an immune therapy drug into the cancer that is intended to promote a participant's own immune system to attack the cancer. The first part of this trial (sub-protocol A) is a phase 1 trial including dose escalation and expansion at one or more doses. It is the first time that ATTR-01 will be given to humans. If an optimal dose is identified, additional sub-protocols will be added by to further elicit whether ATTR-01 may successfully treat cancer. Expanded access is not available.
Trial Locations
Loading…
Loading trial locations…
Facility
City
State
Country
Status
Eligibility Criteria
Inclusion Criteria:
* Consenting male and female adults (18 years of age) with select solid epithelial tumour indications known to have high frequency (75 percent) of αvβ6 integrin receptor expression as detailed in the applicable SP.
* Received and failed/intolerant of Standard of Care (SoC) thera…
Inclusion Criteria:
* Consenting male and female adults (18 years of age) with select solid epithelial tumour indications known to have high frequency (75 percent) of αvβ6 integrin receptor expression as detailed in the applicable SP.
* Received and failed/intolerant of Standard of Care (SoC) therapy where eligible (not including neoadjuvant).
* Tumour lesion (not previously irradiated), suitable for safe pre- and post-treatment biopsies.
* Measurable disease by Response Evaluation Criteria in Solid Tumours (RECIST) Version 1.1.
* Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) of 0 or 1.
* Minimum life expectancy anticipated to be greater than three months
* Willing to undertake appropriate measures of hygiene to prevent any spread of virus and protection of vulnerable individuals.
* Adequate organ function.
* Compliant with requirements for prior treatment washout and contraceptive measures applicable to genetically modified organisms (GMOs) and cancer therapies
* Prior immune checkpoint antibody therapies as single agents or in combination with other anti-cancer agents is permissible.
Exclusion Criteria:
* Significant degree of fibrotic disease, including autoimmune diseases (e.g. systemic lupus, rheumatoid arthritis) or idiopathic and occupation-related pulmonary fibrosis.
* Known prior history of intolerance to anti-programmed cell death protein 1 (PD-1) and/or anti-PD-L1 immunotherapy due to toxicity.
* Has any of the comorbid conditions listed in the detailed protocol exclusion criteria.
Picking one helps us show the most relevant trials first.
Your results are loading in the background — you can
change this any time from the results page.
Set your location to continue
Find My Trials uses your location to surface clinical trials near you.
Add your city or zip code to your profile and try again.