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Clinical Trialsfor AdvancedSolid Tumors

Second Life Therapeutics is a clinical stage company that is developing an entirely new class of adoptive cell therapies with Leukocyte-Tells to overcome advanced solid cancers.

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Ongoing

Clinical Study

Second Life Therapeutics is conducting a Phase 1/2a clinical trial to evaluate the safety and efficacy of off-the-shelf Leukocyte-Tells (SL-28) monotherapy in patients with advanced solid tumors.

About SL-28

SL-28 is an allogeneic, non-genetically modified cell therapy designed to treat a broad range of solid tumors.

Second Life Group

In prior expanded access use,

SL-28 demonstrated

a near-universal response

rate in patients with diverse

advanced solid malignancies

—highlighting its transformative

potential.

Clinical trial
overview

Second Life Ttherapeutics is currently enrolling patients who have been diagnosed with advanced solid tumors in the first-in-human, Phase 1/2a clinical trial (NCT06800313). We are starting with Australian medical sites shortly, then expanding globally. The purpose of this open label, multi-center clinical trial is to evaluate the anti-tumor activity, safety, and pharmacokinetics of, single-agent SL-28 in patients with a diverse array of solid tumors. The study includes an initial Phase 1 dose escalation to determine recommended dose(s) for expansion of SL-28 as a monotherapy and Phase 2 expansion cohorts.

The study will enroll patients with advanced solid tumors, including those who failed previous lines of chemo- 
and immunotherapies.

Eligibility:

  • Age:18+
  • Sex:All
  • StatusRecruiting

The study will enroll patients with the following tumor types:

  • Head and Neck

    • Head and neck squamous cell carcinoma

  • Thoracic

    • Small-cell lung cancer

    • Non-small cell lung cancer

    • Esophageal cancer

  • Gastrointestinal

    • Gastric cancer

    • Liver cancer

    • Colorectal cancer

    • Pancreatic adenocarcinoma

  • Genitourinary

    • Bladder cancer

    • Renal cell carcinoma

    • Prostate cancer

  • Gynecologic

    • Ovarian cancer

    • Endometrial cancer

  • Breast and Skin

    • Breast cancer

    • Melanoma

+

Other

To learn more about the trial, please email to: clinical@secondlifetx.com Further details for healthcare providers can be accessed below: www.clinicaltrials.gov

About SL-28

A New Mechanism of Action

Watch

Leukocyte-Tells (SL-28)

Represent a first-in-class, allogeneic, non-genetically modified cell therapy for advanced solid tumors. For the first time, immune cells have been engineered to modulate Cell Memory through the newly discovered Universal Receptive System and Teazeled (TezR) receptors.

Safety and Efficacy

Represent a first-in-class, allogeneic, non-genetically modified cell therapy for advanced solid tumors. For the first time, immune cells have been engineered to modulate Cell Memory through the newly discovered Universal Receptive System and Teazeled (TezR) receptors.

Disclaimer

Leukocyte-Tells (SL-28) is an investigational drug that has not been approved by any regulatory agency. The safety and effectiveness have not been fully established.

Expanded Access

Right-To-Try

For patient

If you are a patient and have additional questions, please speak with your treating physician.

For doctor

If you are a healthcare provider who 
is interested in learning more about Second Life Therapeutics investigational therapies, or have questions about participation in one 
of our clinical trials, please submit a request to clinical@secondlifetx.com

Expanded Access (Compassionate Use) and Right-To-Try pathways enable patients with serious diseases to receive investigational treatments when they cannot participate in a clinical trial. These investigational drugs are not approved by regulatory bodies such as FDA or EMA, and these products have not yet completed full-length safety and efficiency clinical trials.

Expanded Access/Right-To-Try pathways are realized primarily through our ongoing sponsored and investigator-initiated clinical trials.

We understand the current limitations for patients’ participation in our clinical trials, and are trying to provide access to our investigational therapies to those who can’t wait.

Second Life Therapeutics will evaluate requests for the participation in Expanded Access/Right-To-Try programs. Information regarding our investigational therapies and ongoing clinical trials can be accessed onclinical programs.

Learn more

How to Submit a Request

Physicians can submit a request on behalf of their patient to clinial@secondlifetx.com Requests must include the following information:

( ! )

A brief summary of the patient’s history to support use in the indication.

Consistent with the 21st Century Cures Act, Second Life Therapeutics may revise this policy at any time. Additionally, the posting of this policy by Second Life Therapeutics shall not serve as a guarantee of access to any specific investigational drug by any individual patient. Second Life Therapeutics’ decision to grant or deny a request for expanded access may be modified or reversed by Second Life Therapeutics at any time, and is subject to Second Life Therapeutics’ continuing evaluation of safety and efficacy data of the investigational drug, as well as other considerations related to Second Life Therapeutics’ sustainability, inventory, manufacturing, and clinical development programs.

01

The name, contact information and professional designation, e.g., MD, of the requesting physician,

02

A brief summary of the patient’s history to support use in the indication.

Disclaimer

This website is intended for educational and informational purposes only and does not constitute the provision of medical advice, diagnosis, or treatment. The information presented herein is not a substitute for consultation with a qualified healthcare professional. Individuals should not rely on this information for medical decisions and are encouraged to seek the advice of their physician or other licensed healthcare provider regarding any medical condition or treatment options.This website may contain forward-looking statements relating to Second Life Therapeutics’ research, development programs, and product candidates, including SL-28 (Leukocyte-Tells). Forward-looking statements are based on current expectations and assumptions that are subject to substantial risks, uncertainties, and factors beyond the company’s control. These statements may include, but are not limited to, expectations regarding:

  • the potential clinical effectiveness, safety, or therapeutic benefit of SL-28 (Leukocyte-Tells) in patients with advanced solid tumors or other malignancies;

  • the ability to reproduce clinical outcomes in additional patients or tumor types;

  • the advancement, timing, or outcomes of preclinical studies and clinical trials;

  • regulatory interactions, approvals, and commercialization prospects; and

  • Second Life Therapeutics’ broader plans to transform the treatment landscape for cancer and other diseases.

Actual results may differ materially from those expressed or implied in any forward-looking statements. Such statements speak only as of the date they are made, and Second Life Therapeutics undertakes no obligation to update them except as required by applicable law.

Case reports

Promising Compassionate

Use Results

Case report 1
Case report 2
Case report 3

For patients who have already tried multiple therapeutic options, early clinical results with Leukocyte-Tells (SL-28) offer new hope. Recent data demonstrated durable responses in patients with advanced solid tumors who had previously failed both chemotherapy and immunotherapy. SL-28 therapy was also very well tolerated, with no patients discontinuing due to side effects. These results highlight the transformative potential of SL-28 for patients with diverse tumor types who urgently need new treatment options.

Disclaimer

Leukocyte-Tells (SL-28) is an investigational drug that has not been approved by any regulatory agency. The safety and effectiveness have not been fully established.

Why SL-28
Is Different

01

SL-28 is changing the paradigm of the therapy of advanced solid tumors. It is based on a proprietary technology, for the first time, regulating and orchestrating multiple anticancer processes in immune cells - including Cell Memory - which has never been done before in medical history.

02

SL-28 has multiple novel anticancer mechanisms not found in other cell therapies. SL-28 are non-genetically modified cells, which put them apart from CAR-T, and they are not delivered from the same patient like CAR-T or TIL therapy.

03

SL-28 is a total, standalone type of cell therapy, offering a groundbreaking approach for patients with advanced solid tumors - even those who failed previous therapies and are considered resistant.

How it works

?

SL-28 a paradigm shift in the treatment of advanced solid tumors

Built on our proprietary platform, SL-28 for the first time enables the regulation and orchestration of multiple anticancer pathways within immune cells, which were previously thought to be unmanageable.

SL-28 a paradigm shift in the treatment of advanced solid tumors

03

Built on our proprietary platform, SL-28 for the first time enables the regulation and orchestration of multiple anticancer pathways within immune cells, which were previously thought to be unmanageable.

SL-28 a paradigm shift in the treatment of advanced solid tumors

01

Built on our proprietary platform, SL-28 for the first time enables the regulation and orchestration of multiple anticancer pathways within immune cells, which were previously thought to be unmanageable.

SL-28 a paradigm shift in the treatment of advanced solid tumors

02

Built on our proprietary platform, SL-28 for the first time enables the regulation and orchestration of multiple anticancer pathways within immune cells, which were previously thought to be unmanageable.

Allogeneic, immediate

off-the shelf therapy

Overcoming Delays in Cell Therapy

Most cell-based therapies require harvesting, modifying, and reinfusing a patient’s own cells, a process that can take weeks - or even months. For patients with advanced cancers, this is time they do not have.

Immediate Access with SL-28

SL-28 eliminates these delays. As an off-the-shelf therapy, it is immediately available for patients who need urgent anti- cancer therapy, allowing treatment to begin without the long manufacturing timelines of conventional, autologous cell therapies.

  • Healthy donors

    Leukapheresis

  • Isolate white blood cells (WBC)

  • WBCs ex vivo through activated by targeting novel TezR receptors

    Increased anticancer activity

    Reduced HLA reactivity

  • Scalable Allogeneic 
WBC Manufacturing

    Fill finish of 1000+ doses/batch

  • SL-28 Immediate Infusion for many patients