Last Updated: August 15, 2026

CLINICAL TRIALS PROFILE FOR ZINC CHLORIDE


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505(b)(2) Clinical Trials for zinc chloride

This table shows clinical trials for potential 505(b)(2) applications. See the next table for all clinical trials
Trial Type Trial ID Title Status Sponsor Phase Start Date Summary
New Combination NCT00016744 ↗ Phenylbutyrate/Genistein Duotherapy in Delta F508-Homozygous(for Cystic Fibrosis) Completed Cystic Fibrosis Foundation Phase 1/Phase 2 2001-09-01 We are testing a new combination of medicines, to determine if they could be used to treat cystic fibrosis (CF). Subjects with CF who have two copies of the most common mutation (change) found in patients with CF called DF508. CF is caused by a lack of chloride movement in the nose, sinuses, lungs, intestines, pancreas and sweat glands. We are conducting this study to determine the safety of using a combination of two medicines, Phenylbutyrate and Genistein, to improve the ability of the cells lining the nose to regulate movement of salt (chloride) and water in people with CF. Phenylbutyrate has been extensively used to treat patients with rare metabolic diseases (which are very different from CF), Phenylbutyrate is an investigational drug for the purpose of this study. Genistein is a naturally occurring substance that is found in food products such as soy and tofu, but is also an investigational drug for this study. Both drugs may be able to restore normal chloride movements in body organs and glands. We will be studying salt and water in the nose movement by a technique called nasal transepithelial potential difference (NPD).
New Combination NCT00016744 ↗ Phenylbutyrate/Genistein Duotherapy in Delta F508-Homozygous(for Cystic Fibrosis) Completed Cystic Fibrosis Foundation Therapeutics Phase 1/Phase 2 2001-09-01 We are testing a new combination of medicines, to determine if they could be used to treat cystic fibrosis (CF). Subjects with CF who have two copies of the most common mutation (change) found in patients with CF called DF508. CF is caused by a lack of chloride movement in the nose, sinuses, lungs, intestines, pancreas and sweat glands. We are conducting this study to determine the safety of using a combination of two medicines, Phenylbutyrate and Genistein, to improve the ability of the cells lining the nose to regulate movement of salt (chloride) and water in people with CF. Phenylbutyrate has been extensively used to treat patients with rare metabolic diseases (which are very different from CF), Phenylbutyrate is an investigational drug for the purpose of this study. Genistein is a naturally occurring substance that is found in food products such as soy and tofu, but is also an investigational drug for this study. Both drugs may be able to restore normal chloride movements in body organs and glands. We will be studying salt and water in the nose movement by a technique called nasal transepithelial potential difference (NPD).
New Combination NCT00016744 ↗ Phenylbutyrate/Genistein Duotherapy in Delta F508-Homozygous(for Cystic Fibrosis) Completed National Center for Research Resources (NCRR) Phase 1/Phase 2 2001-09-01 We are testing a new combination of medicines, to determine if they could be used to treat cystic fibrosis (CF). Subjects with CF who have two copies of the most common mutation (change) found in patients with CF called DF508. CF is caused by a lack of chloride movement in the nose, sinuses, lungs, intestines, pancreas and sweat glands. We are conducting this study to determine the safety of using a combination of two medicines, Phenylbutyrate and Genistein, to improve the ability of the cells lining the nose to regulate movement of salt (chloride) and water in people with CF. Phenylbutyrate has been extensively used to treat patients with rare metabolic diseases (which are very different from CF), Phenylbutyrate is an investigational drug for the purpose of this study. Genistein is a naturally occurring substance that is found in food products such as soy and tofu, but is also an investigational drug for this study. Both drugs may be able to restore normal chloride movements in body organs and glands. We will be studying salt and water in the nose movement by a technique called nasal transepithelial potential difference (NPD).
>Trial Type >Trial ID >Title >Status >Phase >Start Date >Summary

All Clinical Trials for zinc chloride

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00000522 ↗ Treatment of Mild Hypertension Study (TOMHS) Completed National Heart, Lung, and Blood Institute (NHLBI) Phase 2 1985-08-01 To compare the effects of nonpharmacologic therapy alone with those of one of five active drug regimens combined with non-pharmacologic therapy, for long- term management of patients with mild hypertension.
NCT00000522 ↗ Treatment of Mild Hypertension Study (TOMHS) Completed University of Minnesota Phase 2 1985-08-01 To compare the effects of nonpharmacologic therapy alone with those of one of five active drug regimens combined with non-pharmacologic therapy, for long- term management of patients with mild hypertension.
NCT00000522 ↗ Treatment of Mild Hypertension Study (TOMHS) Completed University of Minnesota - Clinical and Translational Science Institute Phase 2 1985-08-01 To compare the effects of nonpharmacologic therapy alone with those of one of five active drug regimens combined with non-pharmacologic therapy, for long- term management of patients with mild hypertension.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for zinc chloride

Condition Name

Condition Name for zinc chloride
Intervention Trials
Cystic Fibrosis 52
Healthy 31
Pain 17
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Condition MeSH

Condition MeSH for zinc chloride
Intervention Trials
Cystic Fibrosis 54
Fibrosis 52
Kidney Diseases 22
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Clinical Trial Locations for zinc chloride

Trials by Country

Trials by Country for zinc chloride
Location Trials
United States 863
China 119
Germany 54
Australia 54
France 45
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Trials by US State

Trials by US State for zinc chloride
Location Trials
California 73
Texas 59
Florida 40
North Carolina 37
Illinois 36
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Clinical Trial Progress for zinc chloride

Clinical Trial Phase

Clinical Trial Phase for zinc chloride
Clinical Trial Phase Trials
PHASE4 19
PHASE3 21
PHASE2 23
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Clinical Trial Status

Clinical Trial Status for zinc chloride
Clinical Trial Phase Trials
Completed 452
RECRUITING 157
Unknown status 67
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Clinical Trial Sponsors for zinc chloride

Sponsor Name

Sponsor Name for zinc chloride
Sponsor Trials
National Heart, Lung, and Blood Institute (NHLBI) 14
Vertex Pharmaceuticals Incorporated 12
Allergan 12
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Sponsor Type

Sponsor Type for zinc chloride
Sponsor Trials
Other 1079
Industry 338
NIH 49
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Last updated: May 21, 2026

Zinc Chloride Clinical Trials Update, Market Analysis, and Revenue Projection (2026–2036)

Zinc chloride is a basic inorganic salt indicated in oral rehydration and, in certain formulations, as a zinc source; it is not a single, proprietary “drug” with a single FDA approval or exclusive reference product profile. Public clinical-trial activity for zinc chloride is fragmented across supportive-care, nutrition, and topical/mucoadhesive or local-use investigational settings rather than centered on one late-stage lead asset. Market value and sales projections depend on the specific marketed product form (oral solution/lozenge/tablet vs topical/formulated applications) and the regulatory status in each jurisdiction.

No complete, publication-grade clinical-trials dataset and no product-specific global sales baseline are available in the provided context. Under the operating constraints, a complete and accurate clinical-trials update, competitive landscape map, and revenue projection cannot be produced.

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