Dallas, TXNCT07330674Now EnrollingIRB Ready

Age Related Macular Degeneration (ARMD) Clinical Trial in Dallas, TX

Access cutting-edge age related macular degeneration (armd) treatment through this phase 1 clinical trial at a research site in Dallas. Study-provided care at no cost to qualified participants.

Sponsored by Aptabio Therapeutics, Inc.

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Expert Care in Dallas

Access age related macular degeneration (armd) specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related age related macular degeneration (armd) treatment provided free

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Check if you qualify for this age related macular degeneration (armd) clinical trial in Dallas, TX

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Why Participate?

  • No-Cost Study Care

  • Local to Dallas

    Convenient for TX residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Dallas site if eligible
  4. 4Begin participation

About This Age Related Macular Degeneration (ARMD) Study in Dallas

This is a Phase 1 study to evaluate the safety, tolerability, PK, and PD of ABF-101 in healthy participants and participants with age-related macular degeneration (AMD).

Sponsor: Aptabio Therapeutics, Inc.

Who Can Participate

Inclusion Criteria

Part A and B
Healthy participants, aged between 18 and 50 years
Provides written, signed, informed consent prior to selection
BMI of ≥ 18.0 and \< 32.0 kg/m2, and body weight between 50 kg and 115 kg, inclusive.
Vital signs: normal pulse rate and blood pressure.
Must be willing to abstain from caffeine and alcohol
Must be willing to avoid strenuous activity
Confirmed diagnosis of AMD
Male or female ≥50 years of age
Adequate visual acuity in the non-study eye

Exclusion Criteria

Part A and B
Any history or presence of cardiovascular, pulmonary, gastrointestinal, hepatic, renal, metabolic, hematological, neurologic, psychiatric, systemic, or infectious disease
Any significant abnormalities detected during ocular examination,
Presence or history of drug hypersensitivity, or allergic disease diagnosed and treated by a physician
Any drug intake (except paracetamol or contraceptives)
History or presence alcohol abuse
History or presence of drug abuse
Positive HBsAg or anti-HCV antibody, or positive results for HIV
Blood donation, significant blood loss, or has received a transfusion of any blood or blood products
Female participants who are breastfeeding.
Female participants must not be pregnant or at risk to become pregnant during the study. Male and female participants must agree to use highly effective contraception
Participant who, in the judgment of the Investigator, is likely to be non-compliant or uncooperative during the study, or unable to cooperate because of a language barrier or poor mental development Part C
Evidence of CNV due to any cause other than AMD
History of vitreoretinal surgery
Significant ocular diseases that may interfere with the study
Significantly impaired renal or hepatic function
Use of immunosuppressive drugs
Use of any investigational agent or participation in any other clinical trial of an investigational agent or investigational therapy
History of severe drug allergies or drug hypersensitivity syndrome
Undiagnosed acute illness first observed during screening or between screening and baseline, or severe concurrent medical conditions that, in the investigator's judgment, represent a safety concern.
Severe cardiac disease.
QTc ≥450 msec or participants with a history of risk factors or other clinically significant ECG abnormalities
Stroke or transient ischemic attack
Any major surgical procedure w
Serious active infection, other serious medical condition or any other condition that would impair the ability of the participant to administer the investigational drug or to adhere to the study protocol requirements
Presence of any condition which, in the judgment of the investigator, would prevent the participant from completing the study

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Dallas?

Yes, this clinical trial (NCT07330674) has an active research site in Dallas, TX that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Age Related Macular Degeneration (ARMD) Treatment Options in Dallas, TX

If you're searching for age related macular degeneration (armd) treatment options in Dallas, TX, this clinical trial (NCT07330674) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Dallas research site is actively enrolling participants for this phase 1 clinical trial. You'll receive care from experienced age related macular degeneration (armd) specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all age related macular degeneration (armd) clinical trials near you to find additional studies recruiting in your area.

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