Phase 1 Lymphoma Trial, Recruiting NCT06708897 Sponsor: Lomond Therapeutics Holdings, Inc. Condition: Lymphoma
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Phase 1 Lymphoma Trial, Recruiting

NCT06708897
Recruiting Phase 1

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You are 18 years of age or older (male or female)
  • You have been diagnosed with a blood cancer called CLL or SLL with symptoms, and have already tried at least 2 previous treatments including specific targeted therapies (BTK inhibitor and venetoclax, or you declined venetoclax), OR you have a type of slow-growing lymphoma (such as marginal zone lymphoma or Waldenstrom's macroglobulinemia) and have had at least 2 prior treatments including specific targeted therapies (confirm with trial site for your specific diagnosis)
  • Alternatively, for a different part of the trial: you have symptomatic CLL or SLL, have had at least 1 prior treatment including a BTK inhibitor, and have never received venetoclax
  • Your bone marrow, liver, and kidneys are working well enough based on blood tests done within 7 days before starting the study drug (confirm specific values with trial site)
  • Your general health and ability to care for yourself meets a certain minimum level (confirm with trial site)
  • If you are a woman who could become pregnant, you have a negative pregnancy test within 7 days before starting the study drug, and you agree to use highly effective birth control from signing consent until 90 days after your last dose
  • You are able to understand the study and are willing to sign a consent form

Who may not be able to join:

  • You have an active, aggressive transformation of your blood cancer called Richter's transformation (however, if you were treated for this and have been in remission for more than 2 years with no signs of it returning, you may still be eligible)
  • You have a known allergy or sensitivity to the study drug or any of its ingredients
  • You have significant heart problems, such as moderate-to-severe heart failure, uncontrolled heart disease, a heart attack in the past 6 months, or a heart rhythm problem requiring certain medications
  • You have an active infection with CMV, hepatitis B, or hepatitis C
  • You currently have an active COVID-19 infection (prior COVID-19 is allowed if you fully recovered more than 14 days ago)
  • You have a serious active infection that requires intravenous antibiotics or similar treatment (you may be eligible once the infection clears)
  • You have certain uncontrolled blood conditions affecting red blood cells or platelets that started within the past 28 days
  • You had a bone marrow transplant from a donor less than 4 months ago, or you are still on medications to suppress your immune system after a transplant
  • You have another active cancer that is expected to limit your survival to less than 2 years, or that requires active treatment at the same time as this trial (certain early-stage or hormonally treated cancers may be exceptions — confirm with trial site)
  • You have a physical finding or test result that the doctor believes makes it unsafe for you to participate
  • You still have significant side effects (grade 2 or higher) from a previous cancer treatment that have not resolved (hair loss is an exception)
  • You currently need ongoing immune-suppressing medications, including regular steroid pills or infusions for cancer or other conditions (low-dose steroids or inhaled/topical steroids may be acceptable — confirm with trial site)
  • You had major surgery or a serious injury within 4 weeks before starting the study drug
  • You are currently breastfeeding (you would need to stop breastfeeding before and during treatment, and for at least 3 months after the last dose)
  • You have a specific heart rhythm measurement (called QTcF) that is too prolonged and cannot be corrected with standard measures (confirm with trial site)

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 5 July 2026
Phase 1: approximately ~10% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Phone: +38269728309

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 1
Sponsor
Lomond Therapeutics Holdings, Inc.
Registry
ClinicalTrials.gov
Start date
8 April 2025
Est. completion
1 March 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Incidence of AEs and SAEs

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 5 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov