No insider purchase over the last 90 days. The latest was filed 20 Oct 2022.
This page follows insider dealings at Tricida, Inc. as filed with SEC (Form 4), a company from the Healthcare & Pharma sector based in Menlo Park, United States. The group dates from 2013. No insider at Tricida, Inc. has published a filing in the past twelve months. The most recent one dates from 25 November 2022.
Since 2021, the database holds 19 purchases and 27 sales by insiders of the company.
For comparison within the same sector, see the insider buying recorded at Cooper Companies, Inc. and Cytosorbents Corp. These figures are compiled from regulatory filings published by SEC (Form 4). They describe what insiders did and are not a recommendation.
This score ranks the purchase within its own market. A position size is suggested only on the venues of the backtested strategy universe; elsewhere, signals stay on watch. Not investment advice.
FY ended December 2021 · cache
Same trade as the filing by David P. Bonita, counted once · View ↗
25 of 63 declarations
Tricida, Inc. is a U.S.-based biopharmaceutical company that was historically listed on the Nasdaq market in the United States, specifically on the Nasdaq Global Select Market under the ticker TCDA before its delisting trajectory associated with restructuring proceedings. The company was founded in 2013, incorporated in Delaware, and built its operating footprint in California, with principal offices in South San Francisco. Tricida’s business model centered on a single lead development asset, veverimer (also known as TRC101), an orally administered, non-absorbed polymer designed to treat metabolic acidosis in patients with chronic kidney disease (CKD). In other words, Tricida was primarily a drug-development company rather than a diversified commercial pharmaceutical group, with its corporate value tied to the clinical, regulatory, and financing progress of one main candidate. That focused strategy gave the company a clear therapeutic thesis, but it also concentrated risk: the investment case depended heavily on regulatory acceptance, trial outcomes, and the company’s ability to secure funding long enough to reach commercialization. From a competitive standpoint, Tricida operated in a specialized renal/metabolic niche, competing indirectly with broader CKD-supportive therapies and other medical approaches, while lacking the product breadth, international scale, and commercial infrastructure of large-cap drug makers. Recent corporate history has been dominated by financial distress and restructuring. Tricida filed for Chapter 11 bankruptcy protection on January 11, 2023, and later disclosed plans to deregister its securities with the SEC and suspend reporting obligations. For investors, particularly those tracking SEC Form 4 insider activity, TCDA has been an example of a single-asset biotech with a high-risk, binary profile: promising scientific focus on one side, but substantial exposure on the other side to clinical uncertainty, regulatory setbacks, liquidity pressure, dilution, and eventual loss of exchange trading relevance. Given its U.S. market listing and Nasdaq history, any analysis of Tricida should be framed through the lens of the American public markets and the capital-intensive realities of late-stage biotech development.
Purchases our model currently ranks for the recommendations list.
All recommendationsHeadquarters: Menlo Park, United States · Founded: 2013
Source: Wikidata (CC0).
| Fiscal year end | Revenue | Net income | Diluted EPS | Filing |
|---|---|---|---|---|
| Dec 2021 | n.d. | -176.6 m USD | -3.44 USD | 10-K |
| Dec 2020 | n.d. | -264.8 m USD | -5.29 USD | 10-K |
| Dec 2019 | n.d. | -176.8 m USD | n.d. | 10-K |
| Dec 2018 | n.d. | -102.8 m USD | n.d. | 10-K |
| Dec 2017 | n.d. | -41.3 m USD | n.d. | 10-K |
Amounts in USD, as filed (forms 10-K, 20-F or 40-F). Source: SEC EDGAR.