ClinicalTrials.gg
RecruitingNCT07807345Updated Oct 23, 2026

Phase 1 Study of STRO-006 in Adults With Refractory Solid Tumors That Are Recurrent or Metastatic

A Phase 1 interventional study of STRO-006 and Pembrolizumab in Head & Neck Squamous Cell Carcinoma, Non-Small Cell Lung Cancer and Esophageal Cancer, sponsored by Sutro Biopharma, Inc.. Recruiting at 6 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-23.

Sponsored by Sutro Biopharma, Inc. · Phase 1, Interventional, and Treatment

Updated Oct 23, 2026Now RecruitingSite recruiting status changed+2 moreGo to Updates ↓
Phase
Phase 1
Study type
Interventional
Enrollment
285
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

This study is a first-in-human (FIH) Phase 1 open-label, multicenter study including three parts:

  • Part 1A is a dose escalation of STRO-006 monotherapy in selected tumor types reported to commonly express ITGB6. Part 1A will determine the safety, tolerability, pharmacokinetics (PK), and preliminary anti-tumor activity of STRO-006.
  • Part 1B is a dose expansion in one or more indications, as determined by the Sponsor, to further evaluate a STRO-006 monotherapy dose, examine anti-tumor activity, and determine the recommended Phase 2 dose (RP2D) of STRO-006 monotherapy.
  • Part 1C is a combination dose escalation to determine safety, tolerability, PK, and preliminary anti-tumor activity of STRO-006 combined with pembrolizumab.
02

Conditions studied

  • Head & Neck Squamous Cell Carcinoma
  • Non-Small Cell Lung Cancer
  • Esophageal Cancer
  • Gastric Cancer
  • Colorectal Cancer
  • Endometrial Cancer
  • Urothelial Carcinoma (UC)
  • Breast Cancer

Keywords

  • Integrin beta-6
  • STRO-006
  • Antibody Drug Conjugate
  • ADC
03

In context

Squamous Cell Carcinoma of Head and Neck

2,018 studies on the registry are indexed under Squamous Cell Carcinoma of Head and Neck; 573 are open to participants now.

This study's planned enrollment of 285 is above the median of 48 across 1,653 interventional studies indexed under Squamous Cell Carcinoma of Head and Neck.

Browse Squamous Cell Carcinoma of Head and Neck studies →

Lead sponsor

Sutro Biopharma, Inc. is the lead sponsor of 8 studies on the registry; 2 are open to participants now.

Of its 5 completed or terminated interventional studies of FDA-regulated products, 1 (20%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • or cytologically documented solid tumors that are recurrent or including: HNSCC (excluding EBV-positive nasopharyngeal carcinoma), NSCLC, esophageal/gastric cancer, colorectal cancer, endometrial carcinoma, urothelial carcinoma, and breast cancer (HR-positive [-positive or HER2-negative] and TNBC subtype)
  • Age ≥ 18 years
  • of at least 3 months
  • Willingness and ability to comply with the study protocol and long
  • (ECOG) performance status 0 to 1-term follow-up (LTFU) assessments
  • Has received standard systemic therapies with known clinical benefit, or is considered inappropriate for such therapies, in the opinion of the investigator. In the dose escalation Phases (Parts 1A and 1C), there is no limit on the number of prior therapies
  • Expansion Phase (Part 1B) only: Up to two prior therapies are allowed. For participants with AGA-driven adenocarcinoma NSCLC up to four prior therapies are allowed
  • per v1.1.
  • Adequate hematologic and organ function

Exclusion criteria

Exclusion Criteria:

  • Prior anticancer treatment with an ADC with a TOP1 inhibitor payload. (Prior therapy with an ITGB6-targeted ADC is otherwise allowed.)
  • Prior anticancer therapy (prior to first dose of study treatment): chemotherapy within ≤ 2 weeks, ICI ≤ 3 weeks, ADCs ≤ 3 weeks, palliative radiation therapy ≤ 2 weeks, and major surgery ≤ 4 weeks of C1D1. If not specified, ≥ 5 half-lives or 2 weeks, whichever is longer, since administration of prior therapy must have elapsed
  • Residual (CTCAE) v5 ≥ Grade 2 toxicity from prior anticancer therapy, with the exception of Grade 2 alopecia or Grade 2 peripheral neuropathy, which is controlled, and endocrinopathies secondary to prior ICI controlled by hormonal treatment. For Part 1C only: discontinued prior immunotherapy due to treatment-related toxicity
  • Untreated or active and/or
  • Participants with active ILD or active, non-infectious pneumonitis or a history of active pneumonitis ≤ 6 months from the first dose of study treatment
  • Significant, concurrent renal, hepatic, hematological, gastrointestinal, endocrine, pulmonary, neurological, cerebral, or psychiatric disease that could impact participation in this clinical trial
  • Previous solid organ or bone marrow transplantation
  • Concurrent participation in another therapeutic treatment trial
Terms in these criteria, in plain language(11)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Histologically or cytologically confirmed

The diagnosis was confirmed by looking at a sample under a microscope: tissue from a biopsy or surgery (histology), or cells from a fluid or needle sample (cytology).

Your pathology report is the document that shows this.

Relapsed and refractory

Relapsed: the illness came back after treatment had worked. Refractory: it did not respond to treatment, or stopped responding while still on it.

Metastases

Cancer that has spread from where it began to other parts of the body. “Metastatic” cancer is cancer that has spread this way.

HER2

HER2 is a protein, made from the ERBB2 gene, that drives the growth of some cancers. A study may look for a level of the protein, extra copies of the gene, or a particular change in it.

In breast cancer, protein tests are read as HER2-positive, HER2-low or HER2-negative; other cancers use their own rules. Check which test result the study requires.

Life expectancy

The study doctor’s estimate of how long someone is likely to live. Criteria use it so that people can stay in the study long enough for it to answer its question.

ECOG performance status

A scale of how much an illness limits everyday activity. For people being assessed to join a study, scores run from 0 (fully active) to 4; lower is more active.

0
Fully active, no restrictions.
1
Limited in strenuous activity, but walking and able to do light work, such as housework or office work.
2
Walking and able to look after yourself, but unable to work; up and about more than half of waking hours.
3
Able to look after yourself only in part; in bed or a chair more than half of waking hours.
4
Unable to look after yourself at all; in bed or a chair all day.

Studies most often ask for 0–1 or 0–2. Your doctor gives the score; the WHO scale uses the same steps. The full scale also has 5, which records death.

Measurable disease

The amount of disease can be tracked with a defined measurement, so the study can see whether it shrinks or grows. It might be a tumour measured on a scan or, in some blood cancers such as myeloma, a marker measured in blood or urine.

The criteria or the study team say which measurement counts — having no tumour visible on a scan does not by itself rule you out.

RECIST

The standard rules for measuring tumours on CT or MRI scans, to tell whether a cancer is shrinking, stable or growing during treatment.

“Measurable disease per RECIST 1.1” usually means at least one tumour 10 mm or more at its longest on a CT scan, or a lymph node 15 mm or more across its short axis.

CTCAE grade

The US National Cancer Institute’s scale of how severe an adverse event is — any unwanted medical event during a study, such as a symptom, an illness or an abnormal test result, whether or not a treatment caused it. Whether it did is judged separately.

1
Mild.
2
Moderate.
3
Severe.
4
Life-threatening.
5
Death due to the event.

“Side effects of earlier treatment resolved to grade 1 or less” means they have settled to mild or gone.

Brain metastases

Cancer deposits in the brain from a cancer that started elsewhere in the body (CNS metastases include the spinal cord).

Studies differ: some leave out any brain metastases, some accept ones treated and stable for some weeks. Check what this study allows.

Leptomeningeal disease

Cancer that has spread to the leptomeninges, the thin layers covering the brain and spinal cord, and the fluid between them. It is not the same as brain metastases.

Criteria often treat it separately, and many studies leave it out even where treated brain metastases are allowed.

05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Sequential assignment
Masking
None (open label)
Enrollment
285 participants (estimated)

Study arms

  • Experimental
    Part 1A STRO-006 monotherapy

    Drug: STRO-006

  • Experimental
    Part 1B STRO-006 monotherapy

    Drug: STRO-006

  • Experimental
    Part 1C STRO-006 in combination with pembrolizumab

    Drug: STRO-006 · Drug: Pembrolizumab

Interventions

06

What researchers measure

Primary outcomes

  1. Part 1A, 1C: Incidence and severity of Dost-limiting Toxicities (DLTs)

    Time frame: 21 days

  2. Part 1A, 1C: Incidence and severity of Treatment-Emergent Adverse Events (TEAEs)

    Time frame: 21 days

  3. Part 1B: Objective Response Rate (ORR)

    Time frame: 2.5 years

  4. Part 1B: Disease control rate (DCR)

    Time frame: 2.5 years

  5. Part 1B: Duration of Response (DOR)

    Time frame: 2.5 years

  6. Part 1B: Progression-Free Survival (PFS)

    Time frame: 2.5 years

  7. Part 1B: Rate of OS12

    Time frame: 12 months

  8. Part 1B: Incidence and severity of treatment emergent adverse events and serious adverse events

    Time frame: 21 days

Secondary outcomes

  1. Part 1A, Part 1B, Part 1C: Standard PK parameters for the ADC, total antibody, and exatecan payload following single- and repeat-dose administration.

    Time frame: 2.5 years

  2. Part 1A, Part 1B, Part 1C: Incidence of circulating ADA over time

    Time frame: 2.5 years

  3. Part 1A, 1C: Objective Response rate (ORR)

    Time frame: 2.5 years

  4. Part 1A, Part 1C: Disease control rate (DCR)

    Time frame: 2.5 years

  5. Part 1A, Part 1C: Duration of Response (DOR)

    Time frame: 2.5 years

  6. Part 1A, Part 1C: Progression-Free Survival (PFS)

    Time frame: 2.5 years

  7. Part 1A, Part 1C: Rate of OS12

    Time frame: 1 year

07

Study locations

3 of 6 sites recruiting
08

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedDate before it movedWhere the date was before it movedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Oct 2026 (actual). Primary completion is estimated for Feb 2028, 16 months after the start.

Of 154 industry-sponsored phase 1 interventional studies under Squamous Cell Carcinoma of Head and Neck, half reached primary completion within 52 months of starting (the median), counting those still running; a quarter within 35 and three quarters within 72. This study's planned 16 months is below that.

Counting every sponsor, half of 267 studies reached it within 49 months; a quarter within 33 and three quarters within 66.

Start moved once since we started tracking on Sep 25, 2026: Sep 2026 → Oct 2026, on Oct 23, 2026.

Earlier changes are on the record history on ClinicalTrials.gov ↗

How these figures are worked out, and which studies are left out of them.

Registered
Aug 31, 2026
First posted
Sep 8, 2026
StartActual
Oct 19, 2026was Sep 2026
Primary completionEst.
Feb 2028
CompletionEst.
Dec 2028
Last update
Oct 23, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Status
Not yet recruiting→Recruiting
changed Oct 23, 2026
Sites
1 site removed. 6 sites changed recruiting status (3 now recruiting, 3 now not yet recruiting)
Show 6 sites
  • SCRI at Florida Cancer Specialists · Orlando, United Statesno status→Recruiting
  • Massachusetts General Brigham · Boston, United Statesno status→Not yet recruiting
  • OU Health Stephenson Cancer Center · Oklahoma City, United Statesno status→Not yet recruiting
  • NEXT Oncology Dallas · Irving, United Statesno status→Recruiting
  • Texas Tech University Health Sciences Center · Lubbock, United Statesno status→Not yet recruiting
  • NEXT Oncology Virginia · Fairfax, United Statesno status→Recruiting
Show 1 removed
  • UCSD Moores Cancer Center · La Jolla, United States
Oct 23, 2026
Start date
Sep 14, 2026→Oct 19, 2026 (actual)
Oct 23, 2026
Site contacts
Changed at 1 site. See the sites
Show the site
  • OU Health Stephenson Cancer Center · Oklahoma City, United StatesContact person changed (no phone or email listed)
Oct 23, 2026
Show all 1 update
  1. Oct 23, 2026
    Not yet recruiting→Recruiting
    1 site removed. 6 sites changed recruiting status (3 now recruiting, 3 now not yet recruiting)
    Show 6 sites
    • SCRI at Florida Cancer Specialists · Orlando, United Statesno status→Recruiting
    • Massachusetts General Brigham · Boston, United Statesno status→Not yet recruiting
    • OU Health Stephenson Cancer Center · Oklahoma City, United Statesno status→Not yet recruiting
    • NEXT Oncology Dallas · Irving, United Statesno status→Recruiting
    • Texas Tech University Health Sciences Center · Lubbock, United Statesno status→Not yet recruiting
    • NEXT Oncology Virginia · Fairfax, United Statesno status→Recruiting
    Show 1 removed
    • UCSD Moores Cancer Center · La Jolla, United States
    Start date Sep 14, 2026→Oct 19, 2026 (now actual)
    Site contacts Changed at 1 site. See the sites
    Show the site
    • OU Health Stephenson Cancer Center · Oklahoma City, United StatesContact person changed (no phone or email listed)
    + 1 other change: verification date

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07807345
Lead sponsor
Sutro Biopharma, Inc.
Responsible party
Sponsor
First posted
Sep 8, 2026
Start date
Oct 19, 2026
Primary completion
Feb 2028 (estimated)
Completion
Dec 2028 (estimated)
Last update
Oct 23, 2026

Study contacts

Sutro Clinical Team
Contact
clinicaltrials@sutrobio.com
650-801-6416
Jennifer Oliver
study director · Sutro Biopharma

Oversight

FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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