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Thiocarb (DITIOCARB)
Thiocarb (generic name: DITIOCARB) is a ditiocarb drug. It is currently in Phase 2 development.
Thiocarb works by inhibiting the activity of Gasdermin-D, a protein that plays a key role in the inflammatory response and cell death.
Thiocarb is a small molecule with the chemical name diethyldithiocarbamate. It has been studied in clinical trials for various conditions, including metastatic melanoma, glioma, glioblastoma, and stage IV melanoma, in combination with disulfiram, arsenic trioxide, and copper.
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Baseline phase 2 → approval rate
+15.3pp
Industry-wide phase 2 drugs reach approval ~15.3% of the time (BIO/Informa 2023 industry benchmark across all therapeutic areas).
| Regulator | Country | Likely year | Lag vs FDA |
|---|---|---|---|
| FDA | US | 2031–2034 | — |
| EMA | EU | 2032–2035 | +0.7 yr |
| MHRA | GB | 2032–2035 | +0.7 yr |
| Health Canada | CA | 2032–2036 | +0.9 yr |
| TGA | AU | 2032–2036 | +1.2 yr |
| PMDA | JP | 2032–2036 | +1.5 yr |
| NMPA | CN | 2033–2037 | +2.3 yr |
| MFDS | KR | 2032–2036 | +1.4 yr |
| CDSCO | IN | 2032–2037 | +1.8 yr |
| ANVISA | BR | 2033–2037 | +2.3 yr |
Hover any row for the lag rationale. Lag estimates are reduced when the drug has FDA Breakthrough or EMA PRIME designation (sponsors file globally in parallel).
Estimate based on the BIO/Informa industry phase transition rates plus per-drug modifiers for therapeutic area, sponsor type, FDA designations, mechanism, and trial design. Per-jurisdiction lags from Tufts CSDD international approval studies. Not investment, clinical or regulatory advice. Methodology: /methodology#likelihood.
At a glance
| Generic name | DITIOCARB |
|---|---|
| Drug class | ditiocarb |
| Target | Cytochrome P450 2E1, Gasdermin-D, Histone-lysine N-methyltransferase EHMT1 |
| Modality | Small molecule |
| Therapeutic area | Other |
| Phase | Phase 2 |
Mechanism of action
Think of Gasdermin-D like a switch that turns on inflammation and cell death. Thiocarb is like a key that locks this switch, preventing it from being turned on and reducing inflammation and cell death. This can help to treat conditions where inflammation and cell death are a problem.
Approved indications
Common side effects
- Radiation inflammation
Key clinical trials
- Disulfiram With Copper Gluconate and Liposomal Doxorubicin in Treatment-Refractory Sarcomas (PHASE1)
- A Study of Gefitinib, Trametinib, Disulfiram, and Sunitinib in Addition to Standard Chemotherapy in People With Osteosarcoma (PHASE2)
- Zn-DDC to Target Hypoxia-NFkappaB-CSCs Pathway in Multiple Myeloma
- Anxiety During Abstinence in AUD (EARLY_PHASE1)
- The Effects of Disulfiram (Antabuse®) on Visual Acuity in Patients With Retinal Degeneration (PHASE1)
- Phase II Trial of Disulfiram With Copper in Metastatic Breast Cancer (PHASE2)
- Disulfiram/Copper Combination In The Treatment of Newly Diagnosed Glioblastoma Multiform (PHASE2)
- Disulfiram/Copper With Concurrent Radiation Therapy and Temozolomide in Patients With Newly Diagnosed Glioblastoma (PHASE1,PHASE2)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- Thiocarb CI brief — competitive landscape report
- Thiocarb updates RSS · CI watch RSS
Frequently asked questions about Thiocarb
What is Thiocarb?
How does Thiocarb work?
What is the generic name of Thiocarb?
What drug class is Thiocarb in?
What development phase is Thiocarb in?
What are the side effects of Thiocarb?
What does Thiocarb target?
Related
- Drug class: All ditiocarb drugs
- Target: All drugs targeting Cytochrome P450 2E1, Gasdermin-D, Histone-lysine N-methyltransferase EHMT1
- Therapeutic area: All drugs in Other
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing