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RecruitingNCT07819136Updated Sep 17, 2026

REC-7735 in Participants With Solid Tumors

A Phase 1/2 interventional study of REC-7735 in Solid Tumors, sponsored by Recursion Pharmaceuticals Inc.. Recruiting at 3 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-17.

Sponsored by Recursion Pharmaceuticals Inc. · Phase 1/2, Interventional, and Treatment

Phase
Phase 1/2
Study type
Interventional
Enrollment
90
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The study is designed to characterize the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary anti-tumor activity of REC-7735 in participants with unresectable, locally advanced, or metastatic PIK3CA-H1047R mutated solid tumors.

02

Conditions studied

  • Solid Tumors

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Keywords

  • PIK3CA-H1047R
  • Cancer
03

Who can participate

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

Eligibility criteria

Key Inclusion Criteria:

  • Participants have histologically-confirmed unresectable, locally advanced, or metastatic solid tumors which exhibit the PIK3CA H1047R mutation in tumor tissue and/or blood (circulating tumor deoxyribonucleic acid [ctDNA]).
  • For Phase 1A and planned monotherapy cohorts in Phase 1B, participants have experienced progressive disease, relapsed disease, or be intolerant to at least one established standard systemic anti-cancer treatment for a given tumor type, or in the opinion of the Investigator have been considered ineligible for standard therapy.
  • All toxicities from prior anti-cancer therapies have resolved to ≤ Grade 1 or the participant's previous baseline, with the exception of alopecia and peripheral neuropathy.

Key Exclusion Criteria:

  • Participants have experienced disease progression with a phosphoinositide 3-kinase (PI3Ka), protein kinase B (AKT) or mechanistic target of rapamycin (mTOR) inhibitor unless deemed suitable for REC-7735 treatment at the discretion of the Investigator and following discussion with the Sponsor.
  • Known loss-of-function mutations in phosphatase and tensin homolog (PTEN), PTEN loss, or activating mutations in AKT, unless deemed suitable for REC-7735 treatment at the discretion of the Investigator and following discussion with the Sponsor.
  • Major surgery within 6 weeks from treatment initiation.
  • Any serious underlying medical or psychiatric condition that would preclude understanding and rendering of informed consent or impair the ability of the participant to receive or tolerate the planned treatment.
  • Recent or ongoing serious infection.
  • Recent prior systemic anti-cancer treatment.
  • Known clinically significant UGT1A1 deficiency, including Gilbert's syndrome (for example, documented homozygous UGT1A1*28)
  • Has an established diagnosis of uncontrolled diabetes mellitus defined as meeting any one of the following:

NOTE: This criterion is not applicable to those participants enrolling in the Phase 1B Dose Expansion cohort designated for hyperglycemia vulnerable participants

  • Glycated hemoglobin (HbA1c) ≥8%
  • Currently requiring insulin
  • Fasting blood glucose (FBG) ≥140 milligrams (mg)/deciliter (dL) (7.8 millimoles [mmol]/liter [L]) in the past 30 days prior to dosing

NOTE: Two FBG samples must be drawn at least seven days apart from each other.

Note: Other protocol-defined inclusion/exclusion criteria may apply.

04

Study design

Phase
Phase 1 / Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Sequential assignment
Masking
None (open label)
Enrollment
90 participants (estimated)

Study arms

  • Experimental
    Phase 1A Dose Finding: REC-7735

    Participants will receive REC-7735 twice daily (BID).

    Drug: REC-7735

  • Experimental
    Phase 1B Dose Expansion/Optimization: REC-7735

    Participants will receive REC-7735 BID.

    Drug: REC-7735

Interventions

  • DrugREC-7735

    Oral

05

What researchers measure

Primary outcomes

  1. Phase 1A: Number of Participants With Dose-limiting Toxicities (DLTs)

    Time frame: 28 days

  2. Number of Participants With Treatment-emergent Adverse Events (TEAEs)

    Time frame: Up to 2 years

  3. Phase 1B: Objective Response Rate (ORR) According to Standard Response Evaluation Criteria in Solid Tumors (RECIST) 1.1

    Time frame: Up to 2 years

Secondary outcomes

  1. Maximum (Peak) Drug Concentration (Cmax) of REC-7735

    Time frame: Up to 2 years

  2. Time to Reach Cmax following drug administration (Tmax) of REC-7735

    Time frame: Up to 2 years

  3. Area Under the Concentration-time Curve During a Dosing Interval (AUCtau) of REC-7735

    Time frame: Up to 2 years

  4. Phase 1A: ORR According to Standard RECIST 1.1

    Time frame: Up to 2 years

  5. Phase 1B: Clinical Benefit Rate (CBR) According to Standard RECIST 1.1

    Time frame: Up to 2 years

  6. Phase 1B: Duration of Response (DOR) According to Standard RECIST 1.1

    Time frame: Up to 2 years

  7. Phase 1B: Duration of Stable Disease (SD) According to Standard RECIST 1.1

    Time frame: Up to 2 years

  8. Phase 1B: Time to Response (TTR) According to Standard RECIST 1.1

    Time frame: Up to 2 years

  9. Phase 1B: Progression-free Survival (PFS) According to Standard RECIST 1.1

    Time frame: Up to 2 years

  10. Phase 1B: Overall Survival

    Time frame: Up to 2 years

06

Study locations

1 of 3 sites recruiting
  • START Midwest
    Grand Rapids, Michigan 49546, United States
    Recruiting
  • NEXT Oncology - Dallas
    Irving, Texas 75039, United States
    Not yet recruiting
  • NEXT Virginia
    Fairfax, Virginia 22031, United States
    Not yet recruiting
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07819136
Lead sponsor
Recursion Pharmaceuticals Inc.
Responsible party
Sponsor
First posted
Sep 14, 2026
Start date
Sep 2026 (estimated)
Primary completion
Jan 2031 (estimated)
Completion
Jan 2031 (estimated)
Last update
Sep 17, 2026

Study contacts

Recursion Pharmaceuticals
Contact
clinicaltrials@recursionpharma.com
385-374-1724

Oversight

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

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