Komori
Medinet (2370) · InitiativeReframed

Change in the Use of Proceeds Following the Discontinuation of Argos's Development Program

First written in FY2018-Q3. 10 of 11 entries say "Reframed", first in FY2019-Q3. Latest entry: FY2025.

11entries
8years
0from disclosures
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How it moved
ProgressHeldSoftenedWorseFirst statedFY2018-Q3ReframedFY2019-Q3 – FY20252018: 120182019: 120192020: 120202021: 120212022: 120222023: 320232024: 120242025: 22025
Same theme, other companies
Reallocation of stock acquisition rights proceeds to growth investment and debt repaymentA theme 8 companies write about · 0 as a headwind · 3 as a tailwind

Medinet moved to the "Worse" side of this theme in 2019.

1 other company's latest entry also says "Reframed".

Ridges = years it wrote progress, valleys = years it wrote worse. Most hopeful companies at the back. Drag to turn, scroll to zoom, right-drag to pan. On a phone, two fingers turn and pinch to zoom; one finger scrolls the page.
Full recordFilings, disclosures and news, newest first
  1. FY2025ReframedAnnual report

    「At a meeting of its Board of Directors held on 29 August 2025, the Company resolved to change the expenditure details and scheduled expenditure period set out in the "Changes to the Use of Funds and Scheduled Expenditure Period" disclosed in the 31 March 2023 disclosure titled "(Change to Disclosed Matters) Changes to the Use of Funds and Scheduled Expenditure Period Related to the Issuance of Stock Acquisition Rights Through a Third-Party Allotment."」

    For the 15th and 16th Stock Acquisition Rights, the Company revised the amount and timing of expenditures for the development of glycan-modified T cells and other products, and reallocated unused funds to development costs for new regenerative medicine products.
  2. FY2025-H1ReframedAnnual report

    「We discontinued expenditures after deciding to terminate development of the regenerative medicine product in question. Of the ¥1,192 million in remaining funds, ¥632 million will be reallocated to the development of various seeds for regenerative medicine products currently being pursued, as described in (iii) above. The remaining ¥560 million will be reallocated to working capital for the head office, given the need to secure such funds, as described in (iv) above.」

    Following the discontinuation of development of α-GalCer/DC, ¥632 million of the unused ¥1,192 million was reallocated to seed development for other regenerative medicine products, and ¥560 million to head-office working capital.
  3. FY2024-Q2ReframedAnnual report

    「As the amount expected to be raised will decrease due to the decline in our share price, we reviewed the priority and allocated funds to the use described in (i), for which the originally planned amount and expenditure period remain unchanged.」

    Regarding funds raised through the Series 19 Stock Acquisition Rights, changed the use of proceeds so that head-office working capital would take priority over development costs for chronic heart failure following the decrease in funds expected to be raised due to the decline in the share price. In addition, regarding the unallocated ¥499 million from the Series 17 Stock Acquisition Rights, changed the use from regenerative medicine product development costs to head-office working capital because there are currently no products at a new development stage.
  4. FY2023ReframedAnnual report

    「We will extend the planned expenditure period because additional quality and nonclinical testing is required.」

    For glycan-modified engineered T cells and related research and HSP105-related research, extended the planned expenditure period for the use of proceeds to March 2026 due to research delays and additional testing. Funds for discontinued COVID-19 vaccine development were reallocated to future regenerative medicine product development costs.
  5. FY2023-Q2ReframedAnnual report

    「Delays in executing R&D expenses occurred because research activities fell behind schedule and were temporarily suspended or stalled from March 2020 onward due to the spread of COVID-19. We have evaluated safety in nonclinical safety studies and clinical research conducted under the Act on Securing Safety in Regenerative Medicine and other relevant laws, but will extend the planned expenditure period because additional quality and nonclinical testing is required.」

    Regarding the use of proceeds from the Series 14, Series 15 and Series 16 Stock Acquisition Rights, extended the planned expenditure period for glycan-modified engineered T cells and related research and HSP105-related research to March 2026 due to delays in research progress and interruptions caused by infectious disease. For the Series 17 Stock Acquisition Rights, changed the plan to reallocate part of the funds for the discontinued COVID-19 vaccine development to future regenerative medicine product development costs.
  6. FY2023-Q1ReframedAnnual report

    「Regarding the unallocated ¥322 million of the amount originally planned for expenditure on the joint development, we will change the use of proceeds to joint research toward the commercialization of a regenerative medicine product for treating chronic heart failure with Kyushu University, a national university corporation, announced on 18 November 2019, and to head-office working capital.」

    Changed the use of the unallocated ¥322 million for the BAR-T joint research to joint research costs for chronic heart failure and head-office working capital. Under the use of proceeds from the Series 16 Stock Acquisition Rights, reduced the BAR-T allocation from ¥375 million to ¥53 million and added ¥170 million for chronic heart failure and ¥152 million for head-office working capital.
  7. FY2022ReframedAnnual report

    「This was originally designated as a use of proceeds from the Series 18 Stock Acquisition Rights. However, as the amount raised decreased due to the decline in our share price, no funds were allocated to this use and it had not been implemented, so we will delete it.」

    Changed the use of proceeds from the Series 18 Stock Acquisition Rights and deleted ¥411 million for share acquisitions and other purposes associated with the capital and business alliance. Reduced facility expansion funding from ¥736 million to ¥126 million and changed the plan to prioritize ¥996 million for organizational infrastructure and ¥546 million for head-office working capital.
  8. FY2021-Q3ReframedAnnual report

    「For item ③, the planned amount was changed because funds not used for item ② were allocated to item ③. In addition, because demand for contract manufacturing was lower than initially expected, capacity expansion at the cell processing facility was no longer necessary during the originally scheduled expenditure period, and the planned expenditure period was changed following a review of the timing of capital investment and other factors.」

    Regarding funds raised through the Series 12 Stock Acquisition Rights, reallocated the unused portion of facility consolidation costs to capacity expansion investment and changed the allocated amount and planned expenditure period.
  9. FY2020-Q2ReframedAnnual report

    「Accordingly, at a meeting of the Board of Directors held on 17 January 2020, we resolved to change the use of funds to be raised through the Series 14 and Series 15 Stock Acquisition Rights.」

    Following the discontinuation of joint development of ATL-DC-101, changed the use of proceeds from the Series 14 and Series 15 Stock Acquisition Rights. For Series 14, reduced ATL-DC-101 development costs to ¥3 million and reallocated funds to ¥230 million in joint research costs for a regenerative medicine product for chronic heart failure and other uses. For Series 15, changed the use of proceeds to ¥226 million in joint research costs for chronic heart failure and other uses.
  10. FY2019-Q3ReframedAnnual report

    「We decided to temporarily acquire and cancel the 156,350 unexercised Series 13 Stock Acquisition Rights and reconsider the most appropriate means of raising funds.」

    Regarding the Series 13 Stock Acquisition Rights, announced a policy of acquiring and canceling the 156,350 unexercised rights because the share price had fallen below the minimum exercise price, making the financing difficult to execute, and of reviewing the financing method. The development schedule for NeoCart was also expected to change substantially following the transfer of assets to Medavate.
  11. FY2018-Q3First statedAnnual report

    「Items 1 through 3 above were initially based on costs related to commercializing Argos’s AGS-003. Because Argos has now discontinued development of the product, we changed the use of funds to reflect the actual situation. Items 4 and 5 are new intended uses of funds. Item 4 will cover restructuring costs, including the consolidation and relocation of business offices and costs associated with workforce reductions. Item 5 will cover the commercialization of autologous cultured cartilage regenerative medical product MDNT01, announced on 21 December 2017, and the commercialization of the dendritic cell vaccine ATL-DC-101 for adult T-cell leukemia, announced on 22 March 2018.」

    Following discontinuation of AGS-003 development, the Company revised the original use of funds to reflect actual expenditures and designated ¥300 million for restructuring costs and ¥1,029 million for development of MDNT01 and ATL-DC-101.
Moved together

"Business Structure Centered on Comprehensive Immune Cell Therapy Support Services" moved the same way as this thread, in the same document, in 6 of its 11 moves.

665543★123456
  1. ★This thread
  2. 1Business Structure Centered on Comprehensive Immune Cell Therapy Support Services6×
  3. 2Accumulated Losses and Seven Consecutive Years of Net Losses6×
  4. 3Continued Operating and Ordinary Losses5×
  5. 4Increase in Cash Used in Operating Activities5×
  6. 5Japanese Development and Sales License for NeoCart4×
  7. 6Increasing Uncertainty Due to Rapid Yen Depreciation and Higher Resource and Energy Prices3×

★ is this thread; numbers match the list above. The number on a line is how many documents both moved the same way in; lines between the other threads count the documents they moved together in too. Threads that move together often sit closer.

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