
Transforming biotechnology with cutting-edge innovations.
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Transforming biotechnology with cutting-edge innovations.
Carboxamil (Cromolyn Sodium) delivered by dry powder inhaler in the setting of your own home. No toxicity or side effects. Carboxamil is a FDA approved drug repurposed for stage 3 lung cancer.. Carcinex is actively recruiting for stage 3 lung cancer patients.
Our mission is to build a new oncology ecosystem with our solid tumor cancer drug called Carboxamil. Carboxamil (Cromolyn sodium) is an FDA approved drug that we have repurposed for all solid tumor cancers. Carboxamil will transform the lives of those affected by late- stage cancer where there is no effective treatment.
Expanded access, also referred to as compassionate use, is one potential pathway for people with life-threatening diseases to gain early access to an investigational medicine outside of a clinical trial when no satisfactory alternative treatment is available. Carcinex is offering expanded access/ compassionate use in local advanced stage 3 lung cancer. In alignment with FDA regulation Carcinex considers the following criteria to determine if Carboxamil for local advanced stage 3 lung cancers can be made available.
Inclusion Criteria
Patients with local advanced stage 3 lung cancer will be eligible for the study only if they meet the following criteria:
· Provide written informed consent prior to screening.
· Male or female patients, age ≥ 18 years
· Histological- or cytological-confirmed diagnosis of Lung cancer
· Previous tumor scan location in lung
Exclusion Criteria
· Treatment with another investigational drug, biological agent, or device within 4 weeks (6 weeks for biological agents) before screening or 5 half-lives of study agent, whichever is longer.
· Patients with known pericardial effusion
· Patients with active infection or serious concomitant systemic disorder (for example, heart failure) incompatible with the study (at the discretion of the Investigator)
· Planned concomitant participation in another clinical trial of an experimental agent, vaccine, or device.
· Patients with any other medical condition that in the opinion of the Investigator would make the patient unsuitable for enrollment or could interfere with the patient participating in or completing the study.
· Known allergy or history of serious adverse event with Cromolyn Sodium
It’s important to remember that investigational medicines have not yet received regulatory approval; therefore, their potential risks and benefits are not yet established. Doctors and patients should consider all possible benefits and risks when seeking expanded access to an investigational medicine. We encourage individuals to speak directly with their treating physician regarding current or future options, clinical trials, and expanded access programs.
For questions about Carboxamil (cromolyn Sodium) for the treatment of local advanced stage 3 lung cancers, physicians may contact Carcinex directly at charles@carcinex.org. We anticipate acknowledging receipt of requests for information sent to this email within 5 business days.
Available Expanded Access Programs (EAP)
Carboxamil(cromolyn sodium) for the treatment of local advanced stage 3 lung cancer
Carboxamil, an investigational medicine designed to halt the cancer cascade allowing for T-Cells to search out and destroy the tumors that are present.
If you are a patient, family member, or caregiver wishing to know more about Caboxamil(cromolyn sodium), please discuss this EAP and all treatment options with your treating physician or contact charles@carcinex.org
If you are a treating physician and are seeking information about Carboxamil EAP or would like to request access for a patient, please contact: charles@carcinex.org
Safety and efficacy have not been evaluated or established by any regulatory authorities for the investigation of medicines and indications described above.drugs that have the potential to change lives.

In home care monitored by nurse practitioner with full practice authority in the care of late-stage lung cancer
Our experienced team brings advanced skill, knowledge and utmost passion to every patient.
We will explain on a daily basis and bring the patient up to date on the latest results so each patient will feel secure and comfortable in the study.

Carboxamil is for the treatment of local advanced stage 3 lung cancers administered by inhaler in your own home
.Carboxamil(Cromolyn Sodium) is an FDA approved drug repurposed for local advanced stage 3 lung cancers. Carboxamil has an excellent FDA safety profile with no toxicity or side effects There is no hair loss, no compromised immune system or infections from using Carboxamil. Carboxamil has adaptive immunity where tumors will not return to the same place. FDA Expanded Access/ Compassionate Use

Carboxamil (Cromolyn Sodium) is a repurposed FDA approved drug that is non-toxic with no known side effects, meaning no hair loss, no compromised immune system, no infections from using Carboxamil
Carboxamil binds to receptor GPCR 35 and turns off the cancer cascade. By turning off the cancer cascade like your home faucet NEW tumors cannot form, grow or metastasize allowing for the immune system to destroy the tumors that are present
Carboxamil is delivered directly to the tumor site by a state-or-the-art dry powder inhaler allowing for 100% of Carboxamil drug concentration to destroy the tumors that are present inhibiting tumors from spreading elsewhere. Carboxamil has adaptive immunity where tumor will not return to same place
Carcinex Inc has developed the most advanced early detection biomarkers for solid tumors cancers. These biomarkers have 95% selectivity. These biomarkers are not present in normal tissue

Charles Owen repurposed Carboxamil; for the treatment of local advanced stage lung cancers.
35 years of cancer research
Lab and field research
Animal and human studies
FDA orphan drug designation
2 patents granted
Dedicated life to developing Carboxamil- Lung cancer drug of the future a life
My goal is to build a new oncology ecosystem today-
Nothing is better in life then saving a life

Pharmaceutical scientist and board-certified pharmacist with deep expertise in drug formulation, sterile injectables, large molecule therapeutics, and early stage pharmaceutical development. Proven ability to originate novel formulations from first principles, translate bench-scale concepts into manufacturable dosage forms, and navigate
Pharmaceutical scientist and board-certified pharmacist with deep expertise in drug formulation, sterile injectables, large molecule therapeutics, and early stage pharmaceutical development. Proven ability to originate novel formulations from first principles, translate bench-scale concepts into manufacturable dosage forms, and navigate complex regulatory and quality frameworks. Extensive experience at the intersection of R&D, CMC, sterile manufacturing, and regulatory compliance, with hands-on leadership in cleanroom design, lyophilization, and parenteral drug delivery systems. Recognized for rigorous scientific thinking, technical problem-solving, and the ability to operate independently at a senior level in high-complexity environments.

Licensed AGPC-NP since April 2025 with 17+ years of nursing experience, including 7 years in hospice and geriatric care. Skilled in advanced patient assessment, diagnosis, and treatment, with a proven track record of delivering compassionate, high-quality care. Recognized for strong clinical judgment, excellent communication, and colla
Licensed AGPC-NP since April 2025 with 17+ years of nursing experience, including 7 years in hospice and geriatric care. Skilled in advanced patient assessment, diagnosis, and treatment, with a proven track record of delivering compassionate, high-quality care. Recognized for strong clinical judgment, excellent communication, and collaboration with interdisciplinary teams to achieve optimal patient outcomes
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