Financials
Cash Data
- Monthly Burn
- Burn Trend
- Dilution Risk
- SEC Filing
Key Stats
Upcoming Catalysts
FDA decisions, readouts and PDUFA dates · scored by probability of approval
VTVT Catalyst Timeline
Dated clinical, regulatory and corporate events for vTv Therapeutics Inc.
Catalyst Timeline
Dated clinical, regulatory & corporate events for vTv Therapeutics Inc.
Upcoming catalysts 2
Event history 50
Past FDA Catalysts and PDUFA Decisions
How VTVT actually traded into and out of each decision
| Date | Drug | Catalyst | Stage | Reaction | Event Move % | Best Trade % |
|---|---|---|---|---|---|---|
| 2021-06-30 | HPP737 | Phase 1 topline data readout | Phase 1 |
Drug Pipeline Intelligence
| Drug | Indication | Phase | PTRS | rNPV | Status | Enroll | Velocity | Design | Est. Completion | ML Signal | Last Change |
|---|---|---|---|---|---|---|---|---|---|---|---|
| Cadisegliatin Small moleculeNCT06334133 | Diabetes Mellitus, Type 1 | Phase 3 | ACTIVE NOT_RECRUITING | 150 | May 1, 2027 | ||||||
| Cadisegliatin Small moleculeNCT07616206 | Type 1 Diabetes (T1D) | Phase 2 | NOT YET_RECRUITING | 40 | Jun 1, 2027 | ||||||
| TTP399 Small moleculeCompletedNCT02405260 | Diabetes Mellitus, Type 2 | Phase 2 | COMPLETED | 190 | Sep 1, 2016 | ||||||
| TTP399 Small moleculeCompletedNCT03335371 | Diabetes Mellitus, Type 1 | Phase 1 | COMPLETED | 115 | Jan 6, 2020 |
Clinical Trial Results
Readouts, endpoints and source filings for every VTVT program
| Drug Name | Indication | Phase | Date | Trial Results Summary | Title | Source |
|---|---|---|---|---|---|---|
| HPP737 | psoriasis | Phase 1 | 2021-06-29 | HPP737 was 10-100 fold more potent than apremilast in inhibiting the generation of cytokines/chemokines, depending upon the analyte.Read More | vTv Therapeutics to Participate at the 6th World Psoriasis & Psoriatic Arthritis Conference with Poster Presentation on HPP737Read More |
Inside Trades
| Insider | Side | Shares | Price | Value | Date |
|---|---|---|---|---|---|
| BAKER BROS. ADVISORS LPDirector | Grant/Award | 6,000 6,000 held | $0.00 | 06/26/2026 |
Hedge Fund 13F Activity
Hedge Funds invested in VTVT
| Fund | % of Portfolio | Current MV | Shares Owned | Activity |
|---|---|---|---|---|
| Samsara BioCapital, LLC | 0.9 % (-25 %) | 11.24 M | 298.50 K |
VTVT Institutional Ownership Trends
VTVT Short Interest
Shares sold short, counted twice a month.
Options Data
Option Volume
Option Chain Statistics
| Expiry | Call Vol | Put Vol | Vol P/C | Call OI | Put OI | OI P/C | IV Call | IV Call OI-Wtd | IV Call Vol-Wtd | IV Put | IV Put OI-Wtd | IV Put Vol-Wtd |
|---|
Real-Time Option Chain
| Calls | Strike | Puts | ||||
|---|---|---|---|---|---|---|
| Last | Vol | OI | Last | Vol | OI | |
| No data available | ||||||
Calls vs Puts by Expiry
Competitive positioning
How VTVT ranks across every disease it competes in
VTVT News
vTv Therapeutics Announces Oral Presentation at Breakthrough T1D Clinical and Research Congress 2026
vTv Therapeutics announced an oral presentation by Chief Medical Officer Thomas Strack at the Breakthrough T1D Clinical & Research Congress 2026. The presentation focused on hypoglycemia-related burdens in adults with Type 1 Diabetes (T1D) using automated insulin delivery systems. Cadisegliatin, a novel oral therapy, is being evaluated as an adjunctive treatment for T1D. The findings highlight ongoing challenges in managing hypoglycemia despite advancements in insulin technology.
Read more →vTv Therapeutics Announces FDA Orphan Drug Designation for HPPD in Sickle Cell Disease
vTv Therapeutics announced that the FDA has granted Orphan Drug Designation to HPPD, an oral therapy for sickle cell disease. This designation highlights the urgent need for new treatments in this area. Preclinical studies indicate that HPPD effectively increases fetal hemoglobin and reduces oxidative stress, supporting its development as a novel therapy.
Read more →vTv Therapeutics to Host Virtual KOL Event on Hypoglycemia in Type 1 Diabetes and the Cadisegliatin Phase 3 Program on October 20, 2026
vTv Therapeutics will host a virtual KOL event on October 20, 2026, focusing on hypoglycemia in type 1 diabetes and the cadisegliatin Phase 3 program. Leading experts will discuss the challenges of living with T1D and the ongoing Phase 3 CATT1 trial of cadisegliatin. The event will include a Q&A session and will be available for replay afterward.
Read more →vTv Therapeutics Announces Completion of Enrollment in Phase 3 CATT1 Study of Cadisegliatin in Type 1 Diabetes (T1D)
vTv Therapeutics has completed enrollment in its Phase 3 CATT1 study for cadisegliatin, an oral therapy for Type 1 Diabetes. A total of 166 patients were randomized to evaluate the drug's efficacy and safety. The study aims to assess cadisegliatin's potential to reduce hypoglycemia while improving glycemic control. Topline results are expected in mid-2027.
Read more →vTv Therapeutics Announces Inducement Grants under Nasdaq Listing Rule 5635(c)(4)
vTv Therapeutics has granted 2,500 stock options to a non-executive employee as an inducement for employment, in compliance with Nasdaq Listing Rule 5635(c)(4). The options have an exercise price of $31.44 per share and will vest over four years. The company is advancing cadisegliatin, a potential first-in-class therapy for type 1 diabetes, currently in a Phase 3 trial.
Read more →vTv Therapeutics to Participate in September Investor Conferences
vTv Therapeutics Inc. will participate in two investor conferences in September 2026, showcasing their investigational therapy cadisegliatin for type 1 diabetes. The conferences include the H.C. Wainwright 28th Annual Global Investment Conference and the 5th Annual ROTH Healthcare Opportunities Conference. Cadisegliatin is under investigation as a potential first-in-class treatment and has received Breakthrough Therapy designation from the FDA.
Read more →vTv Therapeutics Reports Second Quarter 2026 Financial Results and Provides Corporate Update
vTv Therapeutics reported its financial results for Q2 2026, highlighting progress in its Phase 3 CATT1 trial for cadisegliatin, an oral treatment for type 1 diabetes. The company expects to complete enrollment by Q3 2026 and has sufficient funds to continue operations until the topline data readout. A Key Opinion Leader event is planned for Q4 2026 to discuss cadisegliatin's potential benefits.
Read more →vTv Therapeutics Announces Inducement Grants under Nasdaq Listing Rule 5635(c)(4) - June 2, 2026
vTv Therapeutics announced the granting of 2,500 stock options to a non-executive employee as an inducement to employment, in line with Nasdaq Listing Rule 5635(c)(4). The options have an exercise price of $34.30 and will vest over four years. The company is focused on developing cadisegliatin, a potential first-in-class oral adjunctive therapy for type 1 diabetes, currently in a Phase 3 trial.
Read more →vTv Therapeutics Reports First Quarter 2026 Financial Results and Provides Corporate Update
vTv Therapeutics reported its financial results for Q1 2026, highlighting progress in its Phase 3 CATT1 trial for cadisegliatin, an oral therapy for type 1 diabetes. The company expects to complete enrollment by Q3 2026 and has a solid cash position to support operations. Additionally, a recent license amendment has strengthened its financial standing.
Read more →vTv Therapeutics to Participate in Upcoming May Investor Conferences
vTv Therapeutics Inc. announced its participation in two upcoming investor conferences in May 2026, focusing on its lead candidate, cadisegliatin, for type 1 diabetes. The company will engage in a fireside chat format at both events, providing updates on its clinical pipeline. Cadisegliatin is currently in a Phase 3 trial and has received Breakthrough Therapy designation from the FDA.
Read more →vTv Therapeutics Announces Inducement Grants under Nasdaq Listing Rule 5635(c)(4) - April 7, 2026
vTv Therapeutics announced the grant of 4,000 stock options to a non-executive employee as part of an inducement to employment under Nasdaq Listing Rule 5635(c)(4). The options have an exercise price of $39.54 and will vest over four years. The company is advancing its lead candidate, cadisegliatin, a potential first-in-class treatment for type 1 diabetes, currently in a Phase 3 trial.
Read more →vTv Therapeutics to Participate in the 38th Annual ROTH Conference
vTv Therapeutics Inc. announced its participation in the 38th Annual ROTH Conference, scheduled for March 22-24, 2026, in Dana Point, CA. The company will engage in a fireside chat and hold one-on-one investor meetings. Cadisegliatin, their lead candidate, is under investigation as a potential first-in-class oral adjunctive therapy for type 1 diabetes and is currently in a Phase 3 trial.
Read more →vTv Therapeutics Announces Fourth Quarter and Full Year 2025 Financial Results and Provides Corporate Update
vTv Therapeutics reported its fourth quarter and full year 2025 financial results, highlighting a net loss of $27 million for the year. The company received an additional $20 million from Newsoara under a licensing agreement and expects to complete enrollment for its CATT1 Phase 3 trial by the third quarter of 2026. vTv has significantly strengthened its financial position, with increased cash reserves allowing for a funding runway beyond the anticipated topline readout. The firm continues to focus on the development of cadisegliatin for type 1 diabetes and has expanded its advisory board to support this effort.
Read more →vTv Therapeutics to Participate in Upcoming Investor Conferences
vTv Therapeutics Inc. announced its participation in two upcoming investor conferences, highlighting its focus on cadisegliatin, a potential first-in-class oral therapy for type 1 diabetes. The company is currently conducting a Phase 3 trial for this drug, which has received Breakthrough Therapy designation from the FDA. However, the safety and efficacy of cadisegliatin remain unproven.
Read more →vTv Therapeutics Amends License Agreement with Newsoara Biopharma Co. Ltd. for PDE4 inhibitor, HPP737
vTv Therapeutics has amended its license agreement with Newsoara Biopharma, granting Newsoara exclusive worldwide rights to develop and commercialize the PDE4 inhibitor HPP737. This strategic move includes a $20 million upfront payment and potential future milestone payments totaling approximately $115 million. The partnership aims to enhance the clinical development of HPP737, which has shown promise in treating inflammation-mediated diseases.
Read more →